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Loon

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For other uses, see Loon (disambiguation).

Divers / loons
Temporal range: ?Late Eocene – Recent (see text)
37–0 Ma
The Pacific loon (Gavia pacifica) is the sister species of the black-throated loon (G. arctica)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Clade: Aequornithes
Order: Gaviiformes
Family: Gaviidae
Coues, 1903[1]
Genus: Gavia
Forster, 1788
Diversity
5 species
Synonyms

Family-level:
Colymbidae Vigors, 1825 (but see text)
Colymbinae Bonaparte, 1831 (but see text)
Urinatores Vieillot, 1818
Urinatoridae Vieillot, 1818[verification needed]
Urinatorides Vieillot, 1818

Genus-level:
Colymbus Linnaeus, 1758 (but see text)
Urinator Lacépède, 1799

The loons (North America) or divers (UK/Ireland) are a group of aquatic birds found in many parts of North America and northern Eurasia (Europe, Asia and debatably Africa). All living species of loons are members of the genus Gavia, family Gaviidae and order Gaviiformes.

Description

The loon, the size of a large duck or small goose, resembles these birds in shape when swimming. Like ducks and geese but unlike coots (which are Rallidae) and grebes (Podicipedidae), the loon's toes are connected by webbing. The bird may be confused with cormorants (Phalacrocoracidae), which are not too distant relatives of divers and like them are heavy set birds whose bellies – unlike those of ducks and geese – are submerged when swimming. Flying loons resemble a plump goose with a seagull's wings, relatively small in proportion to the bulky body. The bird holds its head pointing slightly upwards during swimming, but less so than cormorants do. In flight the head droops more than in similar aquatic birds.

Male and female loons have identical plumage. Plumage is largely patterned black-and-white in summer, with grey on the head and neck in some species. All have a white belly. This resembles many sea-ducks (Merginae) – notably the smaller goldeneyes (Bucephala) – but is distinct from most cormorants which rarely have white feathers, and if so usually as large rounded patches rather than delicate patterns. All species of divers have a spear-shaped bill.

Males are larger on average, but relative size is only apparent when the male and female are together.

In winter plumage is dark grey above, with some indistinct lighter mottling on the wings, and a white chin, throat and underside. The species can then be distinguished by certain features, such as size and colour of head, neck, back and bill, but often reliable identification of wintering divers is difficult even for experts – particularly as the smaller immature birds look similar to winter-plumage adults, making size an unreliable means of identification.[2]

Gaviiformes are among the few groups of birds in which the young moult into a second coat of down feathers after shedding the first one, rather than growing juvenile feathers with downy tips that wear off as is typical in many birds. This trait is also found in tubenoses (Procellariiformes) and penguins (Sphenisciformes), both relatives of the loons.[3]

Behaviour and ecology

Four loons, Wolfe Lake, Ontario.

Loons are excellent swimmers, using their feet to propel themselves above and under water while their wings provide assistance. Because their feet are far back on the body, loons are poorly adapted to moving on land, and usually avoid going onto land, except when nesting.

All loons are decent fliers, though the larger species have some difficulty taking off and thus must swim into the wind to pick up enough velocity to become airborne. Only the red-throated diver (G. stellata) can take off from land. Once airborne, their considerable stamina allows them to migrate long distances southwards in winter, where they reside in coastal waters. North European loons migrate primarily via the South Baltic and directly over land to the Black Sea or Mediterranean. Loons can live as long as 30 years and can hold their breath for as long as 90 seconds while underwater.[4][5]

Diet and feeding

Loons find their prey by sight. They eat mainly fish, supplemented with amphibians, crustaceans and similar mid-sized aquatic fauna. Specifically, they have been noted to feed on crayfish, frogs, snails, salamanders and leeches. They prefer clear lakes because they can more easily see their prey through the water. The loon uses its pointy bill to stab or grasp prey. They eat vertebrate prey headfirst to facilitate swallowing, and swallow all their prey whole.

To help digestion, loons swallow small pebbles from the bottoms of lakes. Similar to grit eaten by chickens, these gastroliths may assist the loon's gizzard in crushing the hard parts of the loon's food such as the exoskeletons of crustaceans and the bones of frogs and salamanders. The gastroliths may also be involved in stomach cleaning as an aid to regurgitation of indigestible food parts.

Loons may inadvertently ingest small lead pellets, released by anglers and hunters, that will contribute to lead poisoning and the loon's eventual death. Jurisdictions that have banned the use of lead shot and sinkers include but are not limited to Maine, New Hampshire, Vermont, some areas of Massachusetts, Yellowstone National Park, Great Britain, Canada, Michigan, and Denmark.[6]

Reproduction

Loons nest during the summer on freshwater lakes and/or large ponds. Smaller bodies of water (up to 0.5 km2) will usually only have one pair. Larger lakes may have more than one pair, with each pair occupying a bay or section of the lake. The red-throated loon, however, may nest colonially, several pairs close together, in small Arctic tarns and feed at sea or in larger lakes, ferrying the food in for the young.[4][5]

Loons mate on land, often on the future nest site, and build their nests close to the water, preferring sites that are completely surrounded by water such as islands or emergent vegetation. Loons use a variety of materials to build their nests including aquatic vegetation, pine needles, leaves, grass, moss and mud. Sometimes, nest material is almost lacking. Both male and female build the nest and incubate jointly for 28 days. If the eggs are lost, the pair may re-nest, usually in a different location. Since the nest is very close to the water, rising water may induce the birds to slowly move the nest upwards, over a meter.[4][5]

  • Great northern loon on the nest
    Great northern loon on the nest
  • Juvenile red-throated diver
    Juvenile red-throated diver
  • Great northern loon feeding its young
    Great northern loon feeding its young

Despite the roughly equal participation of the sexes in nest building and incubation, analysis has shown clearly that males alone select the location of the nest. This pattern has the important consequence that male loons, but not females, establish significant site-familiarity with their territories that allows them to produce more chicks there over time. Sex-biased site-familiarity might explain, in part, why resident males fight so hard to defend their territories.[7]

Most clutches consist of two eggs, which are laid in May or June, depending upon latitude. Loon chicks are precocial, able to swim and dive right away, but will often ride on their parents' back during their first two weeks to rest, conserve heat, and avoid predators.

Chicks are fed mainly by their parents for about six weeks but gradually begin to feed themselves over time. By 11 or 12 weeks, chicks gather almost all of their own food and have begun to fly.[4][5]

Biologists, especially from Chapman University, have extensively studied the mating behaviour of the common loon (G. immer). Contrary to popular belief, pairs seldom mate for life. Indeed, a typical adult loon is likely to have several mates during its lifetime because of territorial takeover. Each breeding pair must frequently defend its territory against "floaters" (territory-less adults) trying to evict at least one owner and seize the breeding site. Territories that have produced chicks in the past year are especially prone to takeovers, because nonbreeding loons use chicks as cues to indicate high-quality territories. One-third of all territorial evictions among males result in the death of the owner; in contrast, female loons usually survive. Birds that are displaced from a territory but survive usually try to remate and (re)claim a breeding territory later in life.[8][9][10][11]

Etymology and taxonomy

Loons calling
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The European Anglophone name "diver" comes from the bird's habit of catching fish by swimming calmly along the surface and then abruptly plunging into the water. The North American name "loon" likely comes from either the Old English word lumme, meaning lummox or awkward person, or the Scandinavian word lum meaning lame or clumsy. Either way, the name refers to the loon’s poor ability to walk on land. The scientific name Gavia refers to seabirds in general.[12]

The scientific name Gavia was the Latin term for the smew (Mergellus albellus). This small sea-duck is quite unrelated to loons and just happens to be another black-and-white seabird which swims and dives for fish. It is not likely that the ancient Romans had much knowledge of loons, as these are limited to more northern latitudes and since the end of the last glacial period seem to have occurred only as rare winter migrants in the Mediterranean region.[13][14]

The term gavia was transferred from the ducks to the loons only in the 18th century. Earlier naturalists referred to the loons as mergus (the Latin term for diving seabirds of all sorts) or colymbus, which became the genus name used in the first modern scientific description of a Gavia species (by Carl Linnaeus) in 1758. Unfortunately, confusion about whether Linnaeus' "wastebin genus" Colymbus referred to loons or grebes abounded, with North American ornithologists using the genus name for grebes and European ones, following Nicholas Aylward Vigors and Richard Bowdler Sharpe, for divers. The International Commission on Zoological Nomenclature tried to settle this issue 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. However, the situation was not completely resolved even then, and the following year the ICZN had to act again to prevent Louis Jean Pierre Vieillot's 1818 almost-forgotten family name Urinatoridae from overruling the much younger Gaviidae. Some eminent ornithologists such as Pierce Brodkorb tried to keep the debate alive but the ICZN's solution has been satisfactory.[14][15][16][17]

Systematics and evolution

All living species are placed in the genus Gavia. Phylogenetically, the five living species can be arranged as follows:[18]

Basal lineage

Black-throated lineage

Black-headed lineage

Relationships

The Paleocene Waimanu (an early member of the Sphenisciformes) resembled loons in some aspects of its head and bill, but it was already flightless and used its feet for steering rather than propulsion

The loons were formerly often considered to be the most ancient of the northern hemisphere bird families; this idea grew basically out of the perceived similarity of shape and (probably) habits between loons and the entirely unrelated extinct Cretaceous order Hesperornithiformes. In particular Enaliornis, which was apparently an ancestral and plesiomorphic member of that order, was sometimes used to support claims of Albian (Early Cretaceous) Gaviiformes.[19][20]

More recently, it has become clear that the Anseriformes (waterfowl) and the Galliformes are the most ancient groups of modern birds. It is possible, though not at all well-supported, that these were distinct by the end of the Albian 100 million years ago (Ma). Loons belong to a more modern radiation. They were once believed to be related to grebes, which are also foot-propelled diving birds, and both species were once classified together under the order Colymbiformes. However, as recently as the 1930s, it was determined that the two groups are not that closely related at all and are merely the product of convergent evolution and adapted in a similar way to a similar ecological niche. The similarity is so strong that even the most modern cladistic analyses of general anatomical features are easily misled into grouping loons and grebes.[19][21][22]

The Sibley-Ahlquist taxonomy still allied the loons with the grebes in its massively paraphyletic "Ciconiiformes", and it is almost certain that the relationships of loons lie with some of the orders placed therein. Namely, other recent authors have considered loons to share a rather close relationship with seabirds such as penguins (Sphenisciformes), tubenoses (Procellariiformes), waders (Charadriiformes) – and perhaps the newly discovered clade Mirandornithes which unites grebes (Podicipediformes) and their closest living relatives, the flamingos (Phoenicopteriformes). It is perhaps notable that some early penguins had skulls and beaks that were in many aspects similar to those of the living and fossil Gaviiformes.[21][23]

Fossil record

Red-throated diver or red-throated loon (G. stellata), the smallest living Gavia species. Some Miocene members of this genus were smaller still.

In prehistoric times, the loons had a more southerly distribution than today, and their fossils have been found in places such as California, Florida and Italy. The conflicting molecular data regarding their relationships is not much resolved by the fossil record; though they seem to have originated at the end of the Late Cretaceous like their presumed relatives, modern loons are only known with certainty since the Eocene. By that time almost all modern bird orders are at least strongly suspected to have existed – if not known from unequivocally identified specimens – anyway.[22]

Colymboides, the oldest unequivocal gaviiform genus known as of 2009, is widely known from early Priabonian – about 37 million years ago (Ma) in the Late Eocene – to Early Miocene (late Burdigalian, less than 20 Ma) limnic and marine rocks of western Eurasia north of the Alpide belt, between the Atlantic and the former Turgai Sea. It is usually placed in the Gaviidae already, but usually[24] in a subfamily Colymboidinae, with the modern-type loons making up the Gaviinae. But the Colymboides material is generally quite distinct from modern loons, and may actually belong in a now-extinct family of primitive gaviiforms. Furthermore, the supposed genus could well be paraphyletic, so that for example Dyspetornis – which is now contained therein – might have to be separated again. A leg of an undescribed small diver was found in the Late Oligocene deposits at Enspel (Germany); it too may or may not belong to Colymboides. Of the crown genus Gavia, nearly ten prehistoric species have been named to date, and about as many undescribed ones await further study. The genus is known from the Early Miocene onwards, and the oldest members them are rather small (some are smaller than the red-throated diver). Throughout the late Neogene, the genus by and large follows Cope's Rule.[25][26]

Fossil in Vienna

List of fossil Gavia

  • Gavia sp. (Early-Middle Miocene of eastern United States)[27]
  • Gavia egeriana Švec, 1982 (Early Miocene of Czechoslovakia ?and Cheswold, Delaware, United States –? Yorktown Early Pliocene of Lee Creek Mine, South Carolina, United States)[28]
  • Gavia schultzi Mlíkovský, 1998 (Middle Miocene of Sankt Margarethen, Austria)[29]
  • Gavia sp. (Calvert Middle Miocene ?or Pleistocene of Maryland, United States) – same as Gavia cf. immer below?[30]
  • Gavia spp. (Middle Miocene of Steinheim, Germany) – three species[29]
  • Gavia brodkorbi Howard, 1978 (Late Miocene of Orange County, United States)[31]
  • Gavia moldavica Kessler, 1984 (Late Miocene of Chişinău, Moldova)[29]
  • Gavia paradoxa Umanska, 1981 (Late Miocene of Čebotarevka, Ukraine)[29]
  • Gavia concinna Wetmore, 1940 (Late Miocene/Early Pliocene of west and east United States)[32]
  • Gavia fortis Olson & Rasmussen, 2001 (Yorktown Early Pliocene of Lee Creek Mine, South Carolina, United States)
  • Gavia sp. (Early Pliocene of Empoli, Italy)[33]
  • Gavia sp. (Early Pliocene of Kerč Peninsula, Ukraine)[29]
  • Gavia palaeodytes Wetmore, 1943 (Bone Valley Early/Middle Pliocene of Pierce, Florida, United States)[34]
  • Gavia howardae Brodkorb, 1953 (Yorktown Early Pliocene of Lee Creek Mine, South Carolina, United States – San Diego Middle[verification needed] Pliocene of San Diego, California, United States)[35]
  • Gavia cf. concinna (San Diego Middle/Late[verification needed] Pliocene of San Diego, California, United States) – two species?[36]
  • Gavia sp. (Early Pleistocene of Kairy, Ukraine)[29]
  • Gavia cf. immer (Pleistocene of California and Florida, United States) – possibly a G. immer paleosubspecies[25]

"Gavia" portisi from the Late Pliocene of Orciano Pisano, Italy, is known from a cervical vertebra that may or may not have been from a loon. If so, it was from a bird slightly smaller than common loon. Older authors were quite sure the bone was indeed from a Gavia and even considered G. concinna a possibly junior synonym of it. This is now regarded as rather unlikely due to the quite distinct range and age. Interestingly, the Early Pliocene Gavia skull from Empoli (Italy) was referred to G. concinna, and thus could conceivably have been of "G." portisi if that was indeed a diver. The holotype vertebra may now be lost, which would make "G." portisi a nomen dubium.[25][37]

In addition, there are some older fossils that are sometimes assigned to the Gaviiformes. From the Late Cretaceous, the genera Lonchodytes (Lance Formation, Wyoming, United States) and Neogaeornis (Quinriquina Formation, Chile) have been described; both are usually allied with orders which are considered related to loons. In particular the latter is still sometimes explicitly proposed as a primitive loon as they both were initially, but other authors consider Neogaeornis a hesperornithiform; note however that neither Gaviiformes nor Hesperornithiformes are known from the Southern Hemisphere or anywhere near it. Lonchodytes was more certainly quite close to loons, but probably closer still to some of the loons' relatives. Of similarly doubtful validity and surrounded by considerable dispute[38] is the supposed Late Cretaceous loon Polarornis (Seymour Island, Antarctica). Eupterornis from the Paleocene of Châlons-sur-Vesle (France) has some features reminiscent of loons, but others seem more similar to Charadriiformes such as gulls (Laridae). A piece of a carpometacarpus supposedly from Oligocene rocks near Lusk, Wyoming, was described as Gaviella pusilla, but this handbone also shows some similarities to the plotopterids which were flightless wing-propelled divers and if these are apomorphic would make an unconvincing member of the Gaviidae (though it still could be a small-winged gaviiform in a yet-undescribed family "Gaviellidae"[39]): while the carpometacarpus in Gavia is somewhat convergent to that of wing-propelled divers, enabling the wings to be used as rudders for quick underwater turns, Colymboides still had an unspecialized plesiomorphic hand. Parascaniornis, sometimes allied to the loons by early authors, was eventually determined to be a junior synonym of the hesperornithiform Baptornis. A supposed mid-Eocene diver fossil form Geiseltal (Germany) was erroneously assigned to Gavia.[40]

Notes and references

  1. ^ Melville, RV & Smith, JDD, ed. (1987). Official Lists and Indexes of Names and Works in Zoology. ICZN. p. 17.{{cite book}}: CS1 maint: multiple names: editors list (link)
  2. ^ Appleby, R.H.; Steve C. Madge & Mullarney, Killian (1986). "Identification of divers in immature and winter plumages". British Birds. 79 (8): 365–391.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ Olson (1985: p. 212)
  4. ^ a b c d Sjölander, S. and Ågren, G (1972). "The reproductive behaviour of the Common Loon". Wilson Bull. 84: 296–308. JSTOR 4160227.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^ a b c d Sjölander, S. and Ågren, G (1976). "The reproductive Behavior of the Yellow-billed Loon, Gavia adamsii. (With G. Ågren)". The Condor. 78 (4): 454–463. doi:10.2307/1367094.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^ For a review of the impact of lead shot and alternatives, see Minnesota Pollution Control Agency (2007): Let's Get the Lead Out! Non-lead alternatives for fishing tackle. For a review of gastrolith function, see Wings, Oliver (2007). "A review of gastrolith function with implications for fossil vertebrates and a revised classification" (PDF). Acta Palaeontologica Polonica. 52: 1–16.
  7. ^ Piper, W.H.; Walcott, C.; Mager, J.N. & Spilker, F. (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.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  8. ^ Piper, W.H.; Evers, D.C.; Meyer, M.W.; Tischler, K.B. & Klich, M. (2000): Do common loons mate for life?: scientific investigation of a widespread myth. In: McIntyre, J. & Evers, D.C. (eds.): Loons: old history and new findings – proceedings of a symposium from the 1997 meeting of the American Ornithologists' Union: 43–49. North American Loon Fund, Meredith, New Hampshire.
  9. ^ Piper, W.H.; Tischler, K B. & Klich, M. (2000). "Territory acquisition in loons: The importance of take-over". Animal Behaviour. 59 (2): 385–394. doi:10.1006/anbe.1999.1295. PMID 10675261.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  10. ^ Piper, W.H.; Walcott, C.; Mager, J.N.; Perala, M.; Tischler, K B.; Harrington, Erin; Turcotte, A. J.; Schwabenlander M. & Banfield, N. (2006). "Prospecting in a Solitary Breeder: Chick Production Elicits Territorial Intrusions in Common Loons". Behavioral Ecology. 17 (6): 881–888. doi:10.1093/beheco/arl021.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  11. ^ Piper, W.H.; Walcott, C.; Mager, J.N. & Spilker, F. (2008b). "Fatal Battles in Common Loons: A Preliminary Analysis". Animal Behaviour. 75 (3): 1109–1115. doi:10.1016/j.anbehav.2007.10.025.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  12. ^ LoonWatch – Loon FAQs | Northland College. Northland.edu. Retrieved on 2013-04-05.
  13. ^ Brodkorb (1963: pp. 223–224)
  14. ^ a b Arnott, W.G. (1964). "Notes on Gavia and Mergvs in Latin Authors". Classical Quarterly (New Series). 14 (2): 249–262. doi:10.1017/S0009838800023806. JSTOR 637729.
  15. ^ Linnaeus, Carl (1758): 68.1. Colymbus arcticus. In: Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis (10th ed., vol. 1): 190 [Latin book]. Lars Salvius, Stockholm ("Holmius"). Digitized version
  16. ^ International Commission on Zoological Nomenclature (ICZN) (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: 147–148.
  17. ^ Brodkorb (1963: p. 223)
  18. ^ Boertmann, D. (1990). "Phylogeny of the divers, family Gaviidae (Aves)". Steenstrupia. 16: 21–36.
  19. ^ a b Stolpe, M. (1935). "Colymbus, Hesperornis, Podiceps:, ein Vergleich ihrer hinteren Extremität". J. Ornithol. (in German). 80 (1): 115–128. doi:10.1007/BF01908745.
  20. ^ Brodkorb (1963: pp. 220–221)
  21. ^ a b Slack, K.E.; Jones, C.M.; Ando, T.; Harrison G.L.; Fordyce R.E.; Arnason, U. & Penny, D. (2006). "Early Penguin Fossils, plus Mitochondrial Genomes, Calibrate Avian Evolution". Mol. Biol. Evol. 23 (6): 1144–1155. doi:10.1093/molbev/msj124. PMID 16533822.{{cite journal}}: CS1 maint: multiple names: authors list (link) Supplementary Material
  22. ^ a b Mayr (2009)
  23. ^ Olson (1985: pp. 212–213), Mayr (2004, 2009)
  24. ^ Some (notably Robert W. Storer) have disagreed, usually because they separated Gaviella in the basalmost subfamily of the Gaviidae and considered Colymboides the ancestor of Gavia. More recent authors generally disagree at least regarding the latter: Storer (1956), Olson (1985), Mayr (2009: pp. 75–76)
  25. ^ a b c Brodkorb (1953)
  26. ^ Brodkorb (1963: pp. 223–225), Olson (1985: pp. 212–213), Mlíkovský (2002: pp. 63–64), Mayr (2009: pp. 75–76)
  27. ^ A tiny loon, smaller and more delicate than even the sympatric contemporary G. egeriana-like birds. Probably a distinct species – sexual dimorphism in loons is not very pronounced: Rasmussen (1998).
  28. ^ A small loon, smaller than G. howardae: Olson (1985: pp. 213–214), Rasmussen (1998), Mlíkovský (2002: p. 63)
  29. ^ a b c d e f Mlíkovský (2002: p. 64)
  30. ^ USNM 16612, distal right tibiotarsus. Smaller than common loon; the polished-bone look and large size of the specimen makes a Miocene origin rather unlikely: Wetmore (1941), Olson (1985: p. 214).
  31. ^ Known from a complete ulna. Slightly larger than G. egeriana, but smaller than G. howardae: Olson (1985: p. 214)
  32. ^ Known from skull and limb bones. Much like a large Pacific loon but stouter and heavy-billed like common loon, and generally possessing apparently plesiomorphic traits that those two species share with the red-throated diver. Has been considered a possible junior synonym of "G." portisi, but this is nowadays considered unlikely: Brodkorb (1953), Mlíkovský (2002: p. 64), and see also at "Gavia" portisi.
  33. ^ Known from a skull very similar to the black-throated diver. Initially assigned to G. concinna, but this is not very likely: Mlíkovský (2002: p. 64), and see also at "Gavia" portisi.
  34. ^ Known from a few limb bones. Roughly similar in size to Pacific loon, but proportions seem to differ and apparently not close to any living species except maybe red-throated loon: Brodkorb (1953).
  35. ^ Maybe closest to Pacific loon but smaller than red-throated diver; might be quite distinct. A supposed record from Florida is probably in error: Brodkorb (1953, 1963: p.224).
  36. ^ Initially in part (specimens LACM 2110, 2142) assigned to G. concinna, but apparently one or two undescribed smaller species, about the size of the Pacific loon: Brodkorb (1953), Mlíkovský (2002: p. 64).
  37. ^ Brodkorb (1963: p. 224), Mlíkovský (2002: pp. 64, 256–257)
  38. ^ See for example the discussions in Mayr (2004, 2009).
  39. ^ Not to be used without quotation marks, as it is not a valid taxon.
  40. ^ Brodkorb (1963: pp. 220–223), Olson (1985), Mlíkovský (2002: pp. 64,259–261), Mayr (2009: p. 20)
  41. ^ Demetracopoulou, D. (1933). "The Loon Woman Myth: A Study in Synthesis". The Journal of American Folklore. 46 (180): 101–128. doi:10.2307/535774. JSTOR 535774.
  42. ^ Stewart, Barry D. (2004): Across The Land: A Canadian Journey Of Discovery. Trafford Publishing. ISBN 1-4120-2276-2, p. 143
  43. ^ Heinrichs, Ann (2003): Minnesota. Compass Point Books. ISBN 0-7565-0315-9, p. 44
  44. ^ Moran, Mark; Sceurman, Mark; Godfrey, Linda S. & Hendricks, Richard D. (2005): Weird Wisconsin: Your Travel Guide to Wisconsin's Local Legends and Best Kept Secrets. Sterling Publishing. ISBN 0-7607-5944-8, p. 78
  45. ^ chapter "Brute Neighbors"
  46. ^ www.loons.com

Bibliography

Recordings

Look up loon in Wiktionary, the free dictionary.
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