|Adult in breeding plumage in Wisconsin|
|In non-breeding plumage in North Carolina|
|Approximate distribution map
The common loon or great northern diver (Gavia immer) is a large member of the loon, or diver, family of birds. Breeding adults have a plumage that includes a broad black head and neck with a greenish, purplish, or bluish sheen, blackish or blackish-grey upperparts, and pure white underparts except some black on the undertail coverts and vent. Non-breeding adults are brownish with a dark neck and head marked with dark grey-brown. Their upperparts are dark brownish-grey with an unclear pattern of squares on the shoulders, and the underparts, lower face, chin, and throat are whitish. The sexes look alike, though males are significantly heavier than females. During the breeding season, loons live on lakes and other waterways in Canada; the northern United States (including Alaska); and southern parts of Greenland and Iceland. Small numbers breed on Svalbard and sporadically elsewhere in Arctic Eurasia. Common loons winter on both coasts of the US as far south as Mexico, and on the Atlantic coast of Europe.
Common loons eat a variety of animal prey including fish, crustaceans, insect larvae, molluscs, and occasionally aquatic plant life. They swallow most of their prey underwater, where it is caught, but some larger items are first brought to the surface. Loons are monogamous; that is, a single female and male often together defend a territory and may breed together for a decade or more. Both members of a pair build a large nest out of dead marsh grasses and other plants formed into a mound along the vegetated shores of lakes. A single brood is raised each year from a clutch of one or two olive-brown oval eggs with dark brown spots which are incubated for about 28 days by both parents. Fed by both parents, the chicks fledge in 70 to 77 days. The chicks are capable of diving underwater when just a few days old, and they fly to their wintering areas before ice forms in the fall.
The common loon is assessed as a species of least concern on the IUCN Red List of Endangered Species. It is one of the species to which the Agreement on the Conservation of African-Eurasian Migratory Waterbirds applies. The United States Forest Service has designated the common loon a species of special status because of threats from habitat loss and toxic metal poisoning in its US range.
The common loon is the provincial bird of Ontario, and it appears on Canadian currency, including the one-dollar "loonie" coin and a previous series of $20 bills. In 1961, it was designated the state bird of Minnesota, and appears on the Minnesota State Quarter.
The common loon is also known as the great northern diver in Eurasia. (Another former name, great northern loon, was a compromise proposed by the International Ornithological Committee.) It is one of five loon species that make up the genus Gavia, the only genus of the family Gaviidae and order Gaviiformes. Its closest relative is another large black-headed species, the yellow-billed loon or white-billed diver (Gavia adamsii). There are no recognized subspecies of the common loon.
Danish zoologist and mineralogist Morten Thrane Brünnich first described the common loon in 1764, as Colymbus immer in his Ornithologia Borealis. The now-defunct genus Colymbus contained grebes as well as loons, and remained in use[a] until the International Commission on Zoological Nomenclature attempted to clarify the nomenclature in 1956 by declaring Colymbus a suppressed name unfit for further use and establishing Gavia, created by Johann Reinhold Forster in 1788, as the valid genus name for the loons.
The current genus name Gavia was the Latin term for an unidentified seabird and the specific immer is derived from a Norwegian name for the bird, similar to the modern Icelandic word "himbrimi". The word may be related to Swedish immer and emmer: the grey or blackened ashes of a fire (referring to the loon's dark plumage); or to Latin immergo, to immerse, and immersus, submerged.
The European name "diver" comes from the bird's practice of catching fish by diving. The North American name "loon" was first recorded in this sense in New Englands Prospect (1634) by William Wood (1580-1639); "The Loone is an ill shap'd thing like a Cormorant". It may be derived from Old Norse lómr, as are modern Swedish and Danish lom, in each case referring to the distinctive call.
The adult common loon can range from 66 to 91 cm (26 to 36 in) in length with a 127 to 147 cm (4 ft 2 in to 4 ft 10 in) wingspan, slightly smaller than the similar yellow-billed loon. On average, it is about 81 cm (32 in) long and has a wingspan of 136 cm (54 in). Its weight can vary anywhere from 2.2 to 7.6 kg (4.9 to 16.8 lb). Sizes vary regionally, especially by body mass, with the smallest bodied loons on average from lower-central Canada and the Great Lakes, while westerly birds are similar or mildly larger, and loons breeding further east can appear to be significantly larger. Furthermore, males average up to nearly 27% more massive than females in some populations. Breeding loons in Maine averaged 4.65 kg (10.3 lb) in females and 5.97 kg (13.2 lb) in males, essentially the same weight as the yellow-billed loon although the yellow-billed is still larger than in linear dimensions (especially bill length) than the Maine loons. In Ontario, 20 females averaged 4.5 kg (9.9 lb) and 20 males averaged 5.46 kg (12.0 lb). In contrast, in the Gulf of Alaska, adults of both sexes reportedly averaged 4.13 kg (9.1 lb). Adult breeding plumage consists of a broad black head and neck with greenish, purplish, or bluish sheen. It has a black bill sometimes with a pale tip, and red eyes. The neck is encircled with a characteristic black ring and has two white necklaces of eight to ten short streaks on the upper foreneck, and a noticeable collar of white, parallel lines forming a large oval on the neck-side. The central lower foreneck is pure white, and the lower neck-sides has longitudinal white lines becoming rows of small spots and black lines becoming very narrow. The upperparts are blackish or blackish grey, and each feather has small white spots on it. The upperwing is blackish and with small white spots on the non-primary coverts, whereas the underwing is paler with white coverts except the long black shaft-streaks on the axillaries. The underparts are pure white, but have some black on the undertail coverts and vent. It has a checkered black-and-white mantle and a blackish tail. The legs are pale grey on the inner half and blackish on the outer half, and the webs between the toes are flesh colored.
Adult non-breeding plumage is brownish with a dark neck and head marked with dark grey-brown. The eyes are surrounded with white, and the eyelids are pale. The bill is mostly pale grey, with a dark culmen and tip, but in early spring the tip may turn whitish. The underparts, lower face, chin, and throat are also whitish. The foreneck is whitish, usually forming wedge-shaped notch in dark neck-sides, and may sometimes reveal a shadowy trace of the neck ring or a pale collar. It has dark brownish grey upperparts with an unclear pattern of squares on the shoulders and some wing coverts spotted with white, which are usually concealed while swimming. The male and the female have similar appearances, although they exhibit sexual dimorphism in their physical dimensions with the male larger and significantly heavier than the female.
The heavy dagger-like bill is evenly tapered and greyish, sometimes having a black tip. The bill colour and angle distinguish this species from the yellow-billed loon. The neck is short and thick. It swims very low in the water, with sometimes only its head held above and horizontal to water. It must run across the water surface to get in flight. During flight, its head is slightly lower than its body, with its feet trailing behind. It has a skeletal structure made up of a number of solid bones (this is usual for the Gaviiformes and penguins but unlike most flying birds which have bones with extensive pneumatization, hollow and filled with air to make the skeleton lighter), which adds weight but helps in diving.
A juvenile often has a dark, brownish-grey nape that may look darker than the pale-edged black feathers. It has a dark grey to black head, neck, and upperparts, with white throat, cheeks, and underparts. During the first winter, the bill shape of the young may not be as fully developed as that of the adult, and during the second winter, it much resembles the breeding adult, but with wing coverts lacking white spots.
The common loon is distinguished from the black-throated loon (G. arctica) and the red-throated loon (G. stellata) mainly by its larger size. It usually has a steeper forehead and a bulging forecrown, somewhat similar to the black-throated loon. Its bill is heavier and the back is paler than its hindneck. It is more difficult to separate from the yellow-billed loon, but its breeding plumage has more white markings on the neck and the squares on its shoulders are usually smaller; the non-breeding plumage has darker neck-sides contrasting more sharply with pale areas and bill colour.
The scaly juvenile plumage is retained until January or February of the year following hatching, when a lengthy moult of head and body feathers gives them a more adult-like appearance. Adults shed all their flight feathers simultaneously around this time, leaving them temporarily flightless, prior to gaining breeding plumage, but second-year birds delay this substantial moult until the summer. The adult winter plumage is attained between October and January by partial moult mainly of head, body and tail feathers.
With improved gene-sequencing technology, a draft genome of the common loon has assembled and identified at least 14,169 common loon genes. 80.7% of chicken genes are found in the common loon genome. The physiological costs of deep-water diving and long distance aerial migration of loons have greatly affected loon evolution. Many identified genes are candidate genes for positive selection since the common loon-chicken split 90 million years ago. It is theorized that these candidate genes are related to hemoglobin affinity for oxygen, solute exchange, immunoglobulin function related to immune defense, nervous system development and a number of molecular pathways related to DNA metabolic function, and G-receptor pathways potentially involved in low-light visual acuity. For example, SLC48A, and SLC20A1 are candidate genes in the Gavia lineage for maintaining homeostasis due to maybe having a role in maintaining ion and pH balance.
Distribution and habitat
Common loons are mainly Nearctic, and breed from 48° N to the Arctic Circle, locally south to 40° N and north to 78° N. During their breeding season in spring and summer, most common loons live on lakes and other waterways in the northern United States and Canada, as well as in southern parts of Greenland, in Iceland, in Svalbard, in Jan Mayen, and in Bear Island in Norway; and in Alaska, to the west, and very rarely in Scotland, to the east. Their summer habitat ranges from wooded lakes to tundra ponds. The lakes must be large enough for flight take-off, and provide a large population of small fish. Deep lakes with warm surface waters, relatively low biological productivity and low turbidity where their fish prey are easy to see are habitats where breeding loons are more successful in raising young. For protection from predators, common loons favour lakes with islands and coves. They are rare visitors to the Arctic coast. They are known to exhibit high breeding site fidelity.
Some common loons remain in Iceland year-round, although most migrate. In North America, they winter mainly along north Atlantic and north-east Pacific coasts, many stopping off on the Great Lakes during their migration. They migrate in the day, starting about two hours after sunrise and flying at altitudes of 1500 to 2700 m above sea level, above the convective and turbulent layer of air. In winter they can be seen on North America coasts as far south as Baja California, Sonora, northern Sinaloa, southern Texas, and rarely northern Tamaulipas. In the east, several thousand winter along western European coasts, probably originating from Iceland, Greenland, and Canada. Their range extends into northwestern Europe from Finland to Portugal and southern and northwestern Spain (Galicia and Asturias), as well as the western Mediterranean off Catalonia, and off Morocco in Africa, although only a few hundred travel as far south as Iberia. Although wintering site fidelity is not well known, annually, adults are observed to return to the same wintering locations in the Pacific Ocean (Morro Bay), the Gulf of Mexico (Barataria Bay), the Atlantic Ocean (Maryland and Massachusetts), and the reservoir Lake Pateros.
They usually winter along coasts and on inland lakes, bays, inlets, and streams, with birds migrating to the nearest body of water that will not freeze over in the winter: western Canadian loons go to the Pacific, Great Lakes loons to the Gulf of Mexico region, eastern Canadian loons to the Atlantic, and some loons to large inland lakes and reservoirs. They appear in most of the inland waters of the United States. The South Carolina coast, the Gulf coast adjacent to the Florida panhandle, and the Atlantic seaboard from Massachusetts to Maine have some of the highest concentrations of common loons. Occasional vagrants are recorded inland in Mexico, in San Luis Potosí and Coahuila, as well as in Chiapas and Oaxaca in the south. They are accidental in northern Japan and the Commander Islands in northwestern Pacific, and Cuba in the West Indies.
The common loon is an expert fisher, catching its prey underwater by diving as deep as 60 m (200 ft). With its large webbed feet, the common loon is an efficient underwater pursuit predator and adroit diver. It needs a long run-up distance to gain momentum for flight take-off, and is ungainly on land, sliding on its belly and pushing itself forward with its legs. Its clumsiness on land is due to the legs being positioned at the rear of its body; the pelvic muscles are well developed, ideal for swimming but not well-suited for walking. When it lands on water, it skims along on its belly to slow down, rather than braking with its feet, as they are set too far back. The common loon swims and dives well, and flies competently for hundreds of kilometres in migration. It flies with its neck outstretched, usually calling a particular tremolo that can be used to identify a flying loon. Its flying speed is as much as 120 km/h (75 mph) during migration.
Fish account for about 80% of the diet of the common loon. It forages on fish of up to 26 cm (10 in) in length, including minnows, suckers, gizzard shad, rock bass, alewife, northern pike, whitefish, sauger, brown bullhead, pumpkinseed, burbot, walleye, bluegill, white crappie, black crappie, rainbow smelt, and killifish. The young typically eat small minnows, and sometimes insects and fragments of green vegetation. The freshwater diet primarily consists of pike, perch, sunfish, trout, and bass; the saltwater diet primarily consists of rock fish, flounder, sea trout, herring, Atlantic croaker, haddock, and Gulf silverside. When there is either a lack of fish or they are difficult to catch, it preys on crustaceans, crayfish, snails, leeches, insect larvae, molluscs, frogs, annelids, and occasionally aquatic plant matter such as pondweed, roots, moss, willow shoots, seeds, and algae. It has also been known to eat ducklings.
The common loon uses its powerful hind legs to propel its body underwater at high speed to catch its prey, which it then swallows head-first. If the fish attempts to evade the common loon, the bird chases it down with excellent underwater manoeuvrability due to its tremendously strong legs. Most prey are swallowed underwater, where they are caught, but some larger prey are first brought to the surface. It is a visual predator, so it is essential to hunting success that the water is clear. It normally dives 4 to 10 m (13 to 33 ft), but has been recorded to dive up to 70 m (230 ft). The average diving time is 42 seconds, but the maximum duration spent underwater is about 1 min (60 s).
The common loon's mating system is serially monogamous; breeding pairs jointly defend a territory consisting of an entire small lake or a protected bay within a large lake. A given male and female remain together throughout a breeding attempt, rear their own biological offspring, reunite each spring, and may breed together for many consecutive years. However, in the event of death or territorial eviction of one pair member by an intruding loon of the same sex, the other pair member quickly establishes a pair bond with the evicting bird. (Hence, most adult loons have two or more different mates during their lives.) Evicting individuals tend to be young males and females (5 to 9 years old), while evicted adults are often those 15 years and older.
Pairs do not remain together during winter; in addition, males usually precede females by a few days to a few weeks during spring migration, settling on their lake once a portion of it becomes ice-free. Copulation takes place ashore, often on the nest site, repeated daily until the eggs are laid. The preceding courtship is very simple, with mutual bill-dipping and dives. The displays towards intruders, such as bow-jumping (an alternation of fencing and bill-dipping postures and rushing (running "along the surface with its wings either folded or half-extended and flapping at about the same speed as when taking off") are often misinterpreted as courtship.
Nesting typically begins in early May. Significantly more nesting sites are found on islands than on mainland shoreline. Breeding pairs patrol their territories routinely, even at night, defending the territory both physically and vocally. Pairs that nested together the preceding year typically reuse the nest site from the previous year, if they hatched chicks successfully there. In contrast, pairs that lost their eggs to a predator usually shift the nest to a new location. This logical behaviour pattern appears to depend upon the male, because breeding pairs consisting of last year's male and a female not present during the preceding year continue to exhibit the behaviour; pairs composed of last year's female and a new male tend to select a new nest site, regardless of the success or failure of the previous year's attempt. Despite the lead role of males in nest site selection, both sexes contribute substantially to nest construction. The nest is about 56 cm (22 in) wide and is constructed out of dead marsh grasses and other indigenous plants, and formed into a mound along the vegetated coasts of lakes greater than 3.7 ha (9.1 acres). After a week of construction in late spring, one parent climbs on top to mold the interior of the nest to the shape of its body. Based on a number of studies, nesting success averages about 40%, and most newly hatched young survive due to parental care.
Eggs from first clutches are typically laid in May or early June, the timing depending largely upon the date that lakes become ice-free and inhabitable. A clutch consists of two (occasionally one) olive-brown oval eggs with dark brown spots. Incubation is carried out jointly by male and female and lasts about 28 days. Loons often place nests along steep lake shorelines where adults can quickly dive underwater when approached by predators. The eggs are about 88 mm (3.5 in) long and 55 mm (2.2 in) wide and the two eggs are laid with an interval of one to three days between them, and hatch asynchronously.
Newly hatched chicks are dark chocolate brown in color and have a white belly. Within hours of hatching, the young begin to leave the nest with the parents, swimming close by and sometimes riding on one parent's back. Parents and chicks initially stay in shallow, isolated bays where the parents are able to defend the chicks better from intruding loons and eagles, which are their main predators. Male parents defend broods consisting of two chicks more vigorously than singleton chicks, chiefly with the territorial yodel call. The chicks are capable of making shallow dives from their first day but make deeper dives as they grow. Fledging takes 70 to 77 days. Usually, only one brood is raised. Both parents feed the chicks live prey from hatching to fledging. As they grow, chicks are able to catch an increasingly large proportion of their diet by themselves; they can feed and fend for themselves after about two months, although many juveniles continue to beg from adults well beyond this age. The parent birds capture small fish and hold them crosswise in their bill, call and approach the chicks with their head lowered so that the chicks can grasp them. If food is scarce, the larger chick may peck its small sibling incessantly; on small lakes with limited food, only one chick often survives. Juveniles leave the breeding ground before ice formation in the fall, weeks after their parents. A pair of loons raising two chicks have been estimated to feed on 423 kg of fish during the five and a half months that they spend in their breeding territory.
Loons exhibit a strong tendency to settle as breeders on a lake that resembles their natal one, a phenomenon termed natal habitat imprinting. This preference is based on two lake attributes: size and pH. The behaviour is puzzling, because it is as strong in loons hatched on small, acidic lakes as those from large lakes of neutral pH. Hence, the former group is exhibiting active preference for lakes that have been shown to result in higher chick mortality and lower breeding success.
The common loon produces a variety of vocalizations, the most common of which are the tremolo, the yodel, the wail, and the hoot. Each of these calls communicates a distinct message. The frequency at which it vocalizes has been shown to vary based on time of day, weather, and season. It is most vocally active between mid-May and mid-June. The wail, yodel, and tremolo calls are sounded more frequently at night than during the day; calls have also been shown to occur more frequently in cold temperatures and when there is little to no rain.
The tremolo call—sometimes called the "laughing" call—is characterized by its short, wavering quality. It often uses this call to signal distress or alarm caused by territorial disputes or perceived threats. It emits a tremulous series of up to 10 rather high notes (hu)-heheheheheheha. It also uses the tremolo to communicate its presence to other loons when they arrive at a lake, often when they are flying overhead. It is the only vocalization used in flight. The tremolo call has varying three levels of intensities that correlate with a loon's level of distress, and the types are differentiated by increasingly higher pitch frequencies added to the call.
The yodel is a long and complex call made only by the male. It is used in the establishment of territorial boundaries and in territorial confrontations, and the length of the call corresponds with the loon's level of aggression. The dominant frequencies in the yodel indicate the body mass and thereby the health of males. A male that occupies a new territory appears to alter its yodel to be clearly distinguishable from the call of the previous territory owner.
A loon's wail is a long call consisting of up to three notes, and is often compared to a wolf's howl. It uses this call to communicate its location to other loons. The call is given back and forth between breeding pairs or an adult and its chick, either to maintain contact or in an attempt to move closer together after being separated. It is a loud aaoo, weee-wea weee-wea weee-wea, or ooo-aaah-éééé.
The hoot is a short, soft call and is another form of contact call. It is a more intimate call than the wail and is used exclusively between small family groups or flocks. The common loon hoots to let other family or flock members know where it is. This call is often heard when the adult loon is summoning its chicks to feed.
Longevity and terminal investment
Considerable information on longevity and survival rates has been collected in the past two decades, owing to the implementation of an efficient capture protocol that permits marking and monitoring of large study populations. A rough preliminary analysis showed that common loons of both sexes survive at an annual rate of over 90% until they reach their mid-20s, but show a survival rate of only about 75% thereafter. However, a second, finer-scaled analysis made clear that male loons begin to show higher mortality, increased territory loss and lower body condition starting at age 15. Perhaps in response to their physical decline, males 15 and older show increased rates of both territorial aggression and territorial vocalization. This age-related shift in behaviour is interpreted as terminal investment, a "go for broke" strategy seen in senescing animals that are attempting to eke out another year or two of breeding before they die.
Predators and parasites
Adult common loons have few predators, although bald eagles will attack incubating birds. Attacks by sharks in winter have also been recorded. When a predator approaches (either the loon's nest or the loon itself), the common loon sometimes attacks the predator by rushing at it and trying to stab it with its dagger-like bill, aiming its attacks either at the predator's abdomen or the back of its head or neck, which may be deadly to predators up to the size of a fox or raccoon.
Eggs are taken by a number of mammals, including American mink, striped skunk, otters, foxes and raccoons, with the latter being responsible for nearly 40% of all nest failures. Birds such as herring gulls, northern ravens and American crows will eat unattended eggs. Because their nests are at the water's edge, common loon eggs are especially vulnerable if the adult is absent.
Internal parasites of the common loon include many species of worms, including flatworms, tapeworms, nematodes and spiny-headed worms. High levels of worms may result from feeding changes due to low availability of fish, and can lead to illness and death. Protozoal infections including one caused by Eimeria gaviae and avian malaria have been recorded in this loon. The black fly Simulium annulus is closely associated with the common loon to which it is attracted to chemicals in the uropygial gland secretions as well as by visual and tactile cues. This fly is detrimental to loons, their preferred hosts, transmitting blood-borne parasites and viruses, and causing nest abandonment when numbers are high. External parasites include ischnoceran feather lice, although these are not found on the bird's head.
Status and conservation
Since 1998, the common loon has been rated as a species of least concern on the IUCN Red List of Endangered Species. This is because it has a large range – more than 20,000 km2 (7,700 sq mi) – and because it has a stable population trend that does not warrant a vulnerable rating. It also has a large population size of 612,000 to 640,000 individuals. The estimated breeding population ranges from 1,400 to 2,600 mature individuals in Europe. Over half of the breeding population in North America is found in Ontario with 97,000 territorial pairs, and in Quebec with 50,000 territorial pairs. About 2,400 individuals occur in each of the maritime provinces of Canada—Nova Scotia and New Brunswick. British Columbia accounts for 25,000 territorial pairs. In far northern Canada, about 50,000 territorial pairs are known to occur, and 12,500 to 15,000 territorial pairs occur in the Prairie Provinces of Alberta, Manitoba, and Saskatchewan. In the United States, the largest breeding population is present in Alaska with 3,600 to 6,000 territorial pairs. The U.S. Great Lakes region has 5,900 to 7,200 territorial pairs which accounts for over half of the breeding population in the United States. There are about 100 territorial pairs in the northwestern U.S. states of Washington, Idaho, Montana, and Wyoming. About 2,250 territorial pairs are found in New England and New York. In winter, 3,500 to 4,500 individuals are found in the United Kingdom, and even fewer individuals are found in the western European coastline and in Iceland. Along the Pacific Coast, about 184,000 to 189,000 adults and 31,000 to 32,000 juveniles are found, and along the Atlantic Coast, 423,000 to 446,000 adults and 72,000 to 76,000 juveniles are found.
The common loon is listed under Appendix II of the Convention on the Conservation of Migratory Species, and in Article I under the European Union (EU) Birds Directive. It is one of the species to which the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) is applied. In Europe it appears in 20 Important Bird Areas (IBAs), including Ireland, Svalbard, mainland Norway, Iceland, Spain, and the United Kingdom. It is also a listed species in 83 Special Protection Areas in the EU Natura 2000 network. The USDA National Forest Service has designated the common loon a species of special status, and in the upper Great Lake regions of the Huron-Manistee, Ottawa, and Hiawatha national forests as a regional forester sensitive species.
Threats to status and conservation
Effects of mercury and acid rain pollution on health and brood productivity
The effects of mercury and acid rain pollution are considered to be among some of the most important factors in the reproductive success of common loons. Across the upper United States and lower Canada, studies have shown that lake acidity tends to increase from west to east likely stemming from fossil fuel combustion that releases mercury and other harmful components of acid rain which are then moved eastward by prevailing winds. Acidification of lakes can lead to decreases in the availability of important elements such as calcium while increasing the mobility of toxic metals such as mercury and lead.
Generally, mercury is most commonly found as methylmercury in nature. Acid rain and mercury levels in aquatic environments are positively correlated as increases in acid rain lead to elevated levels of sulfur oxides that are used by sulfate-reducing bacteria to enhance methylmercury production. Mercury levels and pH are also correlated as experiments have shown that increases in pH are correlated with a decrease in mercury levels. Methylmercury levels are then passed from organism to organism through the food chain with the species at the top being the most effected. In this case, mercury levels are passed in the order of crayfish, zooplankton, pre fish, fish and then the common loon. Resulting from this transmission of mercury, there is a significant positive correlation between mercury levels in fish and mercury levels in male, female, and chick blood of common loons; consequently, an increase in mercury concentration in the blood of common loons and fish was seen with a decrease in pH. Related to this information, it was discovered that mercury concentration differs by sex and age of common loons. Male common loons were found to contain the highest blood mercury concentration likely due to the fact that they tend to consume bigger fish with higher mercury concentrations. Females contained the second highest blood mercury concentration with differences between the males likely being due to the fact that females can expel mercury into the eggs they lay. Juveniles had the lowest blood mercury concentration. Scientists found that the data from juveniles helped to best indicate the local mercury availability as they are fed exclusively from their natal territory.
Elevated levels of mercury have been associated with changes in foraging as well as brooding behavior among adult common loons, especially in higher concentrations. Studies have deduced that elevated levels of mercury in the blood of common loons have detrimental effects on brood productivity. One such study found that brood productivity was reduced by half when female blood mercury levels exceeded 4.3 μg/g and productivity completely failed when female blood mercury levels exceeded 8.6 μg/g. These results are related to fish mercury levels of 0.21 μg/g and 0.41 μg/g, respectively. As mercury levels and pH are correlated, scientists have found that brood success decreases with decreasing pH such that environments with a pH at around 4.5 exhibited reproductive success below a calculated positive growth rate threshold.
Due to elevated mercury levels in lakes that common loons inhabit, many studies have revealed that a large number of common loons tested are at high risk for detrimental impacts on health and reproduction. One study in the Adirondack Mountains in New York State showed that 21% of male and 8% of female common loons were at high risk for detrimental impacts. In addition, a study conducted on common loons in Québec, Canada determined that 33% of the loons tested were at high risk for detrimental effects on health and reproduction. Although there have been reductions in recent years in acidifying emissions, there has been limited biological recovery in these lakes most likely due to climate change. Research has shown that warmer summer temperatures can inhibit reestablishment of cold-water fish species in acidified lakes and droughts brought on by increased summer temperatures can further acidify lakes.
Breeding range decline
The common loon's breeding range has moved northward, the species breeding as far south as Iowa a century ago. It too is adversely affected by acid rain and pollution, as well as lead poisoning from fishing sinkers (especially those that are about the size of the grit stones they ingest) and mercury contamination from industrial waste. Heavy metals such as mercury may be partially removed through biological processes such as excretion or deposition in feathers, but their adverse effects are magnified through concentration of the toxic elements in organs such as the liver. Eggs shells may also contain metal contaminants, leading to low reproductive productivity. High levels of heavy metals are linked to loons being in poor condition, males being affected more because they eat larger fish.
The common loon has also faced a decline in breeding range due to hunting, predation, and water-level fluctuations, or flooding. Some environmentalists attempt to increase nesting success by mitigating the effects of some of these threats, namely terrestrial predation and water-level fluctuations, through the deployment of rafts in the loon's breeding territories. In addition, artificial floating nesting platforms have been provided for the common loon in some lakes to reduce the impact of changing water levels due to dams and other human activities. The common loon abandons lakes that fail to provide suitable nesting habitat due to shoreline development. It is endangered by personal water-craft and powerboats that may drown newly born chicks, wash eggs away, or swamp nests. It is still considered an "injured" species in Alaska as a result of the Exxon Valdez oil spill.
The voice and appearance of the common loon has made it prominent in several Native American tales. These include an Ojibwe story of a loon that created the world, and a Micmac saga describing Kwee-moo, the loon who was a special messenger of Glooscap (Glu-skap), the tribal hero. The tale of the loon's necklace was handed down in many versions among Pacific Coast peoples. The Delaware in the east of North America and the Buryats of Siberia also had creation stories involving the loon.
Folk names for the common loon include "big loon", "call-up-a-storm", "greenhead", "hell-diver", "walloon", "black-billed loon", "guinea duck", "imber diver", "ring-necked loon", and "ember-goose". An old colloquial name from New England was call-up-a-storm, as its noisy cries supposedly foretold stormy weather. Some old Scottish names such as arran hawk and carara are corruptions of old Scottish Gaelic onomatopoeic names representing the bird's call; others, like bishop and ember goose, were used to avoid older names for this sometimes ill-omened bird.
The common loon appears on Canadian currency, including the one-dollar "loonie" coin and the previous series of $20 bills. It is the provincial bird of Ontario. It was designated the state bird of the U.S. state of Minnesota in 1961, and also appears on the Minnesota State Quarter. Major League Soccer club Minnesota United FC uses the loon in its crest and nickname.
This bird is central to the plot of the children's novel Great Northern? by Arthur Ransome (in which it is referred to throughout as "great northern diver", with the obsolete scientific name Colymbus immer). The story is set in the Outer Hebrides, where the main characters—a group of children on holiday—notice a pair of divers apparently nesting there. Checking their bird book, they believe that these are great northern divers. However, these have not previously been seen to nest in northern Scotland, and so they ask for help from an ornithologist. He confirms that these birds are indeed the great northern; unfortunately, it soon transpires that he does not wish merely to observe, but wants to steal the eggs and add them to his collection; and to do this, he must first kill the birds. Published in 1947, the story is one where the conservationists are the eventual victors over the egg collector, at a time when the latter hobby was not widely considered to be harmful.
In the 2016 Pixar movie Finding Dory, a somewhat bedraggled and dimwitted loon named Becky is persuaded to use a bucket to help two of the main characters, Nemo and Marlin, get into a marine life institute where the titular Dory is trapped.
- For example, this 1951 British Birds article
- BirdLife International (2018). "Gavia immer". IUCN Red List of Threatened Species. 2018: e.T22697842A132607418.
- Carboneras, C; Christie, D.A.; Garcia, E.F.J. (2016). del Hoyo, Josep; Elliott, Andrew; Sargatal, Jordi; Christie, David A.; de Juana, Eduardo (eds.). "Common Loon (Gavia immer)". Handbook of the Birds of the World Alive. Lynx Edicions. Retrieved 7 November 2016.
- Lovette, Irby J.; Fitzpatrick, John W. (2016). Handbook of Bird Biology. New York, NY: John Wiley and Sons. p. 13. ISBN 978-1-118-29104-7.
- Boertmann, D. (1990). "Phylogeny of the divers, family Gaviidae (Aves)". Steenstrupia. 16 (3): 21–36.
- Gill, Frank; Donsker, David, eds. (2018). "Loons, penguins, petrels". World Bird List Version 8.2. International Ornithologists' Union. Archived from the original on 27 April 2020. Retrieved 12 November 2018.
- Brünnich, Morten Thrane (1764). Ornithologia Borealis (in Latin). Hafnia (Copenhagen): J.C. Kall. p. 38.
- Shufeldt, R.W. (1914). "On the oology of the North American Pygopodes" (PDF). The Condor. 16 (4): 169–180. doi:10.2307/1362079. JSTOR 1362079.
- International Commission on Zoological Nomenclature (1957–58). "The family-group names "Gaviidae" Coues, 1903 and "Urinatoridae" (correction of "Urinatores)" Vieillot, 1818 (Class Aves) – "Opinion" 401 and "Direction" 75". Bulletin of Zoological Nomenclature. 15A: 147–48.
- Jobling, James A. (2010). The Helm Dictionary of Scientific Bird Names. London: Christopher Helm. pp. 171, 203. ISBN 978-1-4081-2501-4.
- Johnsgard 1987, p. 94.
- Johnsgard 1987, p. 107.
- "Diver". Oxford English Dictionary (Online ed.). Oxford University Press. (Subscription or participating institution membership required.)
- "Loon". Oxford English Dictionary (Online ed.). Oxford University Press. (Subscription or participating institution membership required.)
- Wood, William (1865) . Wood's New-England's Prospect. Boston: Prince Society. p. 34.
- "Loom". Oxford English Dictionary (Online ed.). Oxford University Press. (Subscription or participating institution membership required.)
- Lockwood 1984, p. 97.
- Brodkorb, Pierce (1953). "A review of the Pliocene loons" (PDF). Condor. 55 (4): 211–14. doi:10.2307/1364769. JSTOR 1364769.
- Evers, D.C.; Paruk, J.D.; McIntyre, J.W.; Barr, J.F. (2010). Poole, A.F. (ed.). "Common Loon (Gavia immer)". The Birds of North America. Cornell Lab of Ornithology.
- Spahr, Robin (1991). Threatened, endangered, and sensitive species of the Intermountain region. United States Department of Agriculture, Forest Service, Intermountain Region. pp. 115–116.
- Evers, D. C., J. D. Paruk, J. W. McIntyre, and J. F. Barr (2010). Common Loon (Gavia immer), version 2.0. In The Birds of North America (A. F. Poole, Editor). Cornell Lab of Ornithology, Ithaca, NY, USA.
- Storer, R. W. (1988b). Variation in the Common Loon (Gavia immer). In Papers from the 1987 Conference on Common Loon Research and Management., edited by P. I. V. Strong, 54-65. Meredith, NH: North American Loon Fund.
- Dunning, John B. Jr., ed. (2008). CRC Handbook of Avian Body Masses (2nd ed.). CRC Press. ISBN 978-1-4200-6444-5.
- Hunt Jr, G. L., Drew, G. S., Jahncke, J., & Piatt, J. F. (2005). Prey consumption and energy transfer by marine birds in the Gulf of Alaska. Deep Sea Research Part II: Topical Studies in Oceanography, 52(5-6), 781-797.
- Dunne, Pete (2013). Pete Dunne's Essential Field Guide Companion: A Comprehensive Resource for Identifying North American Birds. Houghton Mifflin Harcourt. p. 89. ISBN 978-0-544-13568-0.
- Smith, Nathan D. (2012). "Body mass and foraging ecology predict evolutionary patterns of skeletal pneumaticity in the diverse "waterbird" clade". Evolution. 66 (4): 1059–1078. doi:10.1111/j.1558-5646.2011.01494.x. PMID 22486689. S2CID 42793145.
- "The Uncommon Loon". Wisconsin Department of Natural Resources. Retrieved 2 June 2013.
- Kaufman, Kenn (2011). Kaufman Field Guide to Advanced Birding: Understanding What You See and Hear. Boston, MA: Houghton Mifflin Harcourt. pp. 171–172. ISBN 978-0-547-24832-5.
- Appleby, R.H.; Madge, S.C.; Mullarney, Killian (1986). "Identification of divers in immature and winter plumages" (PDF). British Birds. 79 (8): 365–391.
- Gayk, Zach G., et al. (2018)" Genomic insights into natural selection in the common loon (Gavia immer): evidence for aquatic adaptation." BMC Evolutionary Biology, 18 (1) accessed 17 Apr. 2020.
- Snow, David; Perrins, Christopher M., eds. (1998). The Birds of the Western Palearctic (BWP) concise edition (2 volumes). Oxford: Oxford University Press. pp. 8–10. ISBN 978-0-19-854099-1.
- Thompson, Stephanie A.; Price, J. Jordan (2006). "Water clarity and diving behavior in wintering common loons". Waterbirds. 29 (2): 169–175. doi:10.1675/1524-4695(2006)29[169:wcadbi]2.0.co;2. JSTOR 4132565.
- "All About Birds: Common Loon". Cornell Lab of Ornithology. Archived from the original on 25 May 2017. Retrieved 6 August 2017.
- Arctic National Wildlife Refuge: final comprehensive conservation plan, environmental impact statement, wilderness review, and wild river plans. United States Fish and Wildlife Service, Region 7. 1988. p. 450.
- Paruk, James D; Chickering, Michael D.; Long, Darwin; Uher-Koch, Hannah; East, Andrew; Poleschook, Daniel; Gumm, Virginia; Hanson, William; Adams, Evan M. (2015). "Winter site fidelity and winter movements in common loons (Gavia immer) across North America". The Condor. 117 (4): 485–493. doi:10.1650/CONDOR-15-6.1.
- Kerlinger, Paul (1982). "The migration of common loons through eastern New York" (PDF). The Condor. 84 (1): 97–100. doi:10.2307/1367828. JSTOR 1367828.
- Rappole, John H; Blacklock, Gene W. (1994). Birds of Texas: A Field Guide. College Station, TX: Texas A&M University Press. p. 14. ISBN 978-0-89096-545-0.
- Peterson, Roger Tory; Chalif, Edward L. (1999). A Field Guide to Mexican Birds: Mexico, Guatemala, Belize, El Salvador. Boston, MA: Houghton Mifflin Harcourt. p. 3. ISBN 978-0-395-97514-5.
- Garfield, Eagle; Mesa, Gunnison; Pitkin, Moffat; Routt, Rio Blanco; Colorado, Summit Counties (2002). White River National Forest (N.F.), Land and Resource Management Plan: Environmental Impact Statement. United States Forest Service. p. 62.
- Wilcox, Harry Hammond (1952). "The pelvic musculature of the loon, Gavia immer". The American Midland Naturalist. 48 (3): 513–573. doi:10.2307/2422198. JSTOR 2422198.
- Sandilands, Al (2011). Birds of Ontario: Habitat Requirements, Limiting Factors, and Status: Volume 1–Nonpasserines: Loons through Cranes. Vancouver: University of British Columbia Press. p. 171. ISBN 978-0-7748-5943-1.
- Gibson, J.W. (2007). "Gavia immer Brünnich Common Loon" (PDF). Michigan Natural Features Inventory. Michigan State University. pp. 1–6.
- Eastman, John (2000). The Eastman Guide to Birds: Natural History Accounts for 150 North American Species. Mechanicsburg, PA: Stackpole Books. p. 219. ISBN 978-0-8117-4552-9.
- Piper, Walter H.; Brunk, Kristin M.; Flory, Joel A.; Meyer, Michael W. (2017). "The long shadow of senescence: age impacts survival and territory defense in loons". Journal of Avian Biology. 48 (8): 1062–1070. doi:10.1111/jav.01393.
- Piper, Walter H.; Evers, David C.; Meyer, Michael W.; Tischler, Keren B.; Kaplan, Joseph D.; Fleischer, Robert C. (1997). "Genetic monogamy in the common loon (Gavia immer)". Behavioral Ecology and Sociobiology. 41 (1): 25–31. doi:10.1007/s002650050360. S2CID 33036050.
- Piper, Walter H.; Tischler, Keren B.; Klich, Margaret (2000). "Territory acquisition in loons: the importance of take-over". Animal Behaviour. 59 (2): 385–394. doi:10.1006/anbe.1999.1295. PMID 10675261. S2CID 23085958.
- Piper, Walter H.; Mager, John N.; Walcott, Charles; Furey, Lyla; Banfield, Nathan; Reinke, Andrew; Spilker, Frank; Flory, Joel A. (2015). "Territory settlement in common loons: no footholds but age and assessment are important". Animal Behaviour. 104: 155–163. doi:10.1016/j.anbehav.2015.03.013. S2CID 53404673.
- Piper, Walter H.; Brunk, Kristin M.; Jukkala, Gabriella L.; Andrews, Eric A.; Yund, Seth R.; Gould, Nelson G. (2018). "Aging male loons make a terminal investment in territory defense". Behavioral Ecology and Sociobiology. 72 (6). doi:10.1007/s00265-018-2511-9. S2CID 46956208.
- McIntyre, Judith (1988). The Common Loon: Spirit of Northern Lakes. Minneapolis, MN: University of Minnesota Press. p. 9. ISBN 978-0-8166-1651-0.
- Sjölander, Sverre; Ågren, Greta (1972). "Reproductive behavior of the common loon" (PDF). Wilson Bulletin. 84 (3): 296–308. JSTOR 4160227.
- Sjölander, S.; Ågren, G. (1976). "Reproductive behavior of the yellow-billed loon, Gavia adamsii" (PDF). The Condor. 78 (4): 454–463. doi:10.2307/1367094. JSTOR 1367094.
- Cramp 1977, p. 61.
- Radomski, Paul J.; Carlson, Kristin; Woizeschke, Kevin (2014). "Common loon (Gavia immer) nesting habitat models for north-central Minnesota lakes". Waterbirds. 37 (sp1): 102–117. doi:10.1675/063.037.sp113.
- Paruk, James D. (2008). "Nocturnal behaviour of the common loon, Gavia immer". Canadian Field-Naturalist. 122: 70–72. doi:10.22621/cfn.v122i1.548.
- Rodriguez, R. (2002). "Gavia immer (common loon)". Animal Diversity Web. Archived from the original on 14 July 2017. Retrieved 14 July 2017.
- Piper, Walter H.; Walcott, Charles; Mager, John N.; Spilker, Frank J. (2008). "Nestsite selection by male loons leads to sex-biased site familiarity". Journal of Animal Ecology. 77 (2): 205–210. doi:10.1111/j.1365-2656.2007.01334.x. PMID 17976165.
- Eastman, John Andrew (1999). Birds of Lake, Pond, and Marsh: Water and Wetland Birds of Eastern North America. Mechanicsburg, PA: Stackpole Books. p. 216. ISBN 978-0-8117-2681-8.
- McIntyre, Judith W. (1983). "Nurseries: a consideration of habitat requirements during the early chick-rearing period in common loons". Journal of Field Ornithology. 54 (3): 247–253. JSTOR 4512827.
- Jukkala, Gabriella; Piper, Walter (2015). "Common loon parents defend chicks according to both value and vulnerability". Journal of Avian Biology. 46 (6): 551–558. doi:10.1111/jav.00648.
- Barr, J.F. (1996). "Aspects of common loon (Gavia immer) feeding biology on its breeding ground". Hydrobiologia. 321 (2): 119–144. doi:10.1007/bf00023169. S2CID 32804759.
- Piper, Walter H.; Grear, Jason S.; Meyer, Michael W. (2012). "Juvenile survival in common loons Gavia immer: effects of natal lake size and pH". Journal of Avian Biology. 43 (3): 280–288. doi:10.1111/j.1600-048x.2012.05633.x.
- Piper, Walter H.; Palmer, Michael W.; Banfield, Nathan; Meyer, Michael W. (2013). "Can settlement in natal-like habitat explain maladaptive habitat selection?". Proceedings of the Royal Society of London B: Biological Sciences. 280 (1765): 20130979. doi:10.1098/rspb.2013.0979. PMC 3712445. PMID 23804619.
- Mennill, Daniel J. (2014). "Variation in the vocal behavior of common loons (Gavia immer): Insights from landscape-level recordings". Waterbirds. 37 (sp1): 26–36. doi:10.1675/063.037.sp105.
- "Loon Vocalizations: What are you hearing and what does it mean?". Vermont Fish and Wildlife. Archived from the original on 13 September 2014. Retrieved 27 August 2017.
- Barklow, William E. (1979). "Graded frequency variations of the tremolo call of the common loon (Gavia immer)" (PDF). The Condor. 81 (1): 53–64. doi:10.2307/1367857. JSTOR 1367857.
- Mager III, John N; Walcott, Charles; Piper, Walter H (2012). "Male common loons signal greater aggressive motivation by lengthening territorial yodels". Wilson Journal of Ornithology. 124 (1): 73–80. doi:10.1676/11-024.1. S2CID 85216811.
- Mager, John N.; Walcott, Charles; Piper, Walter H. (2007). "Male common loons, Gavia immer, communicate body mass and condition through dominant frequencies of territorial yodels". Animal Behaviour. 73 (4): 683–690. CiteSeerX 10.1.1.483.1889. doi:10.1016/j.anbehav.2006.10.009. S2CID 43610342.
- Walcott, Charles; Mager, John N.; Piper, Walter (2006). "Changing territories, changing tunes: male loons, Gavia immer, change their vocalizations when they change territories" (PDF). Animal Behaviour. 71 (3): 673(11). doi:10.1016/j.anbehav.2005.07.011. S2CID 43750841.
- Evers, David (1993). A replicable capture method for adult and juvenile common loons on their nesting lakes. In: 1992 Conference on the Loon and Its Ecosystem. Meredith, NH, USA: North American Loon Fund.
- Davies, William E. (2004). "About the cover. Common loon" (PDF). Bird Observer. 32 (3): 202–204.
- Daoust, Pierre-Yves; Conboy, Gary; McBurney, Scott; Burgess, Neil (1998). "Interactive mortality factors in common loons from maritime Canada". Journal of Wildlife Diseases. 34 (3): 524–531. doi:10.7589/0090-3558-34.3.524. PMID 9706561. S2CID 24447180.
- Klnsella, J.M.; Forrester, Donald J. (1999). "Parasitic helminths of the common loon, Gavia immer, on its wintering grounds in Florida" (PDF). Journal of the Helminthological Society of Washington. 66 (1): 1–6.
- Montgomery, Roy D.; Novilla, Meliton N.; Shillinger, Robert B. (1978). "Renal coccidiosis caused by Eimeria gaviae n. sp. in a common loon (Gavia immer)". Avian Diseases. 22 (4): 809–814. doi:10.2307/1589663. JSTOR 1589663. PMID 749899.
- Martinsen, Ellen S.; Sidor, Inga F.; Flint, Sean; Cooley, John; Pokras, Mark A. (2017). "Documentation of malaria parasite (Plasmodium spp.) infection and associated mortality in a common loon (Gavia immer)". Journal of Wildlife Diseases. 53 (4): 859–863. doi:10.7589/2016-08-195. PMID 28665230. S2CID 4391165.
- Weinandt, Meggin L.; Meyer, Michael; Strand, Mac; Lindsay, Alec R. (2012). "Cues used by the black fly,Simulium annulus, for attraction to the common loon (Gavia immer)". Journal of Vector Ecology. 37 (2): 359–364. doi:10.1111/j.1948-7134.2012.00239.x. PMID 23181860. S2CID 768681.
- Piper, Walter H.; Tischler, Keren B.; Reinke, Andrew (2018). "Common loons respond adaptively to a black fly that reduces nesting success". The Auk. 135 (3): 788–797. doi:10.1642/auk-17-239.1. S2CID 90934731.
- Rothschild, Miriam; Clay, Theresa (1953). Fleas, Flukes and Cuckoos. A Study of Bird Parasites. London: Collins. p. 153.
- Franson, J.C.; Cliplef, David J. (1992). "Causes of mortality in common loons". Proceedings from the 1992 Conference on the Loon and its Ecosystem: Status, management, and environmental concerns. US Fish and Wildlife Service. pp. 2–12.
- "Gavia immer | AEWA". Archived from the original on 16 August 2016. Retrieved 12 July 2017.
- Tischler, Keren B. (2011). "Species Conservation Assessment for the Common Loon (Gavia immer) in the upper Great Lakes" (PDF). USDA Forest Service, Eastern Region: 1–59.
- Bianchini, Kristin; Tozer, Douglas C.; Alvo, Robert; Bhavsar, Satyendra P.; Mallory, Mark L. (October 2020). "Drivers of declines in common loon (Gavia immer) productivity in Ontario, Canada". Science of the Total Environment. 738: 139724. Bibcode:2020ScTEn.738m9724B. doi:10.1016/j.scitotenv.2020.139724. PMID 32531589.
- Tozer, Douglas C.; Falconer, C. Myles; Badzinski, Debbie S. (2013). "Common Loon Reproductive Success in Canada: the West is Best but Not for Long". Avian Conservation and Ecology. 8 (1): art1. doi:10.5751/ACE-00569-080101. ISSN 1712-6568.
- Graveland, Jaap (1 March 1998). "Effects of acid rain on bird populations". Environmental Reviews. 6 (1): 41–54. doi:10.1139/a98-003. ISSN 1181-8700.
- Champoux, L.; Masse, D. C.; Evers, D.; Lane, O. P.; Plante, M.; Timmermans, S. T. A. (September 2006). "Assessment of mercury exposure and potential effects on common loons (Gavia immer) in Québec". Hydrobiologia. 567 (1): 263–274. doi:10.1007/s10750-006-0066-7. ISSN 0018-8158. S2CID 10621451.
- Yu, Xue; Driscoll, Charles T.; Montesdeoca, Mario; Evers, David; Duron, Melissa; Williams, Kate; Schoch, Nina; Kamman, Neil C. (October 2011). "Spatial patterns of mercury in biota of Adirondack, New York lakes". Ecotoxicology. 20 (7): 1543–1554. doi:10.1007/s10646-011-0717-y. ISSN 0963-9292. PMC 3175042. PMID 21691858.
- Schoch, Nina; Glennon, Michale J.; Evers, David C.; Duron, Melissa; Jackson, Allyson K.; Driscoll, Charles T.; Ozard, John W.; Sauer, Amy K. (April 2014). "The Impact of Mercury Exposure on the Common Loon ( Gavia immer ) Population in the Adirondack Park, New York, USA". Waterbirds. 37 (sp1): 133–146. doi:10.1675/063.037.sp116. ISSN 1524-4695. S2CID 85674745.
- Burgess, Neil M.; Meyer, Michael W. (February 2008). "Methylmercury exposure associated with reduced productivity in common loons". Ecotoxicology. 17 (2): 83–91. doi:10.1007/s10646-007-0167-8. ISSN 0963-9292. PMID 18038272. S2CID 40571426.
- Wiland, L. (2007). "Common Loon Conservation Status- Migratory Birds of the Great Lakes – University of Wisconsin Sea Grant Institute". Archived from the original on 12 July 2017. Retrieved 12 July 2017.
- Franson, J. Christian; Hansen, Scott P.; Pokras, Mark A.; Miconi, Rose (2001). "Size characteristics of stones ingested by common loons". The Condor. 103 (1): 189–191. doi:10.1650/0010-5422(2001)103[0189:scosib]2.0.co;2. JSTOR 1369696.
- Locke, L.N.; Kerr, S.M.; Zoromski, D. (1982). "Lead poisoning in common loons (Gavia immer)". Avian Diseases. 26 (2): 392–396. CiteSeerX 10.1.1.514.3406. doi:10.2307/1590110. JSTOR 1590110. PMID 7103895.
- Burger, Joanna; Pokras, Mark; Chafel, Rebecca; Gochfeld, Michael (1994). "Heavy metal concentrations in feathers of common loons (Gavia immer) in the northeastern United States and age differences in mercury levels". Environmental Monitoring and Assessment. 30 (1): 1–7. doi:10.1007/BF00546196. PMID 24213705. S2CID 24178181.
- Scheuhammer, Anton M.; Wong, Allan H.K.; Bond, Della (1998). "Mercury and selenium accumulation in common loons (Gavia immer) and common mergansers (Mergus merganser) from Eastern Canada". Environmental Toxicology and Chemistry. 17 (2): 197–201. doi:10.1002/etc.5620170209.
- Desorbo, Christopher R; Taylor, Kate M.; Kramar, David E.; Fair, Jeff; Cooley, John H.; Evers, David C.; Hanson, William; Vogel, Harry S.; Atwood, Jonathan L. (2007). "Reproductive advantages for common loons using rafts". Journal of Wildlife Management. 71 (4): 1206–1213. doi:10.2193/2006-422. ISSN 0022-541X. S2CID 85992979.
- McIntyre, Judith W.; Mathisen, John E. (1977). "Artificial islands as nest sites for common loons". The Journal of Wildlife Management. 41 (2): 317–319. doi:10.2307/3800613. JSTOR 3800613.
- Svingen, Peder H.; Hertzel, Anthony X. (2000). The Common Loon: Population Status and Fall Migration in Minnesota. Minnesota Ornithologists' Union. p. 1.
- Leland, Charles Godfrey (2012). The Algonquin Legends Of New England (Annotated ed.). Jazzybee Verlag. p. 48. ISBN 978-3-8496-2265-7.
- Stallcup, Rich; Evens, Jules (2014). Field Guide to Birds of the Northern California Coast. Berkeley, CA: University of California Press. p. 60. ISBN 978-0-520-27616-1.
- Cocker, Mark; Mabey, Richard (2005). Birds Britannica. London: Chatto & Windus. pp. 306–307. ISBN 978-0-7011-6907-7.
- Bloch, Dorete (2006). Fróðskaparrit 53. Faroe University Press. p. 53. ISBN 978-99918-41-03-8.
- Sandrock, James; Prior, Jean C. (2014). The Scientific Nomenclature of Birds in the Upper Midwest. Iowa City, IA: University of Iowa Press. p. 63. ISBN 978-1-60938-225-4.
- McAtee, W.L (1951). "Bird names connected with weather, seasons, and hours". American Speech. 26 (4): 268–278. doi:10.2307/453005. JSTOR 453005.
- Lockwood 1984, pp. 24, 30, 39, 58.
- Grzimek, Bernhard; Schlager, Neil (2003). Grzimek's Animal Life Encyclopedia, Volume 8: Birds I. Gale. p. 161. ISBN 978-0-7876-6571-5.
- Townsley, Frank (2016). British Columbia: Graced by Nature's Palette. FriesenPress. p. 191. ISBN 978-1-4602-7773-7.
- Carlson, Bruce M (2007). Beneath the Surface: A Natural History of a Fisherman's Lake. Minnesota Historical Society. p. 159. ISBN 978-0-87351-578-8.
- Noles, Jim (2009). A Pocketful of History: Four Hundred Years of America—One State Quarter at a Time. Da Capo Press. ISBN 978-0-7867-3197-8.
- La Vaque, David (27 October 2016). "Minnesota United to donate portion of 2017 season ticket purchases to help loons". Star-Tribune. Minneapolis. Retrieved 8 September 2017.
- McGinnis, Molly (February 2004). "Totem Animals in Swallows & Amazons: Great Northern?". All Things Ransome. Retrieved 26 March 2010.
- Hardyment, Christina (1984). Arthur Ransome & Captain Flint's Trunk. London: Jonathan Cape. pp. 201–204. ISBN 978-0-224-02989-6.
- Scott, A.O. (15 June 2016). "Review: In 'Finding Dory,' a Forgetful Fish and a Warm Celebration of Differences". The New York Times. Archived from the original on 11 May 2017. Retrieved 14 August 2017.
- Wolcott, James (1982). "Big frogs, small pond". Texas Monthly. 10 (1): 120.
- Cramp, Stanley; et al., eds. (1977). "Gavia immer Great Northern Diver". Handbook of the Birds of Europe the Middle East and North Africa. The Birds of the Western Palearctic. Volume I: Ostrich to Ducks. Oxford: Oxford University Press. pp. 56–61. ISBN 978-0-19-857358-6.
- Johnsgard, Paul A. (1987). Diving Birds of North America. Lincoln, NE: University of Nebraska Press. ISBN 978-0-8032-2566-4.
- Lockwood, W.B. (1984). Oxford Book of British Bird Names. Oxford: Oxford University Press. ISBN 978-0-19-214155-2.
|Wikimedia Commons has media related to the common loon.|
|Wikispecies has information related to Gavia immer.|
- Common Loon stamps – bird-stamps.org
- Common loon (Gavia immer) – ARKive
- "Great Northern Diver (Gavia immer) media". Internet Bird Collection.
- The Loon Preservation Committee
- Common loon photo gallery at VIREO (Drexel University)