|in Whitby, Ontario, Canada|
|Part of the range of M. melodia Breeding range Year-round range Wintering range|
Adult song sparrows have brown upperparts with dark streaks on the back and are white underneath with dark streaking and a dark brown spot in the middle of the breast. They have a brown cap and a long brown rounded tail. Their face is gray with a brown streak through each eye. They are highly variable in size across numerous subspecies (for subspecies details, see below). The body length ranges from 11 to 18 cm (4.3 to 7.1 in) and wingspan can range from 18 to 25.4 cm (7.1 to 10.0 in). Body mass ranges from 11.9 to 53 g (0.42 to 1.87 oz). The average of all races is 32 g (1.1 oz) but the widespread nominate subspecies (M. m. melodia) weighs only about 22 g (0.78 oz) on average. The maximum lifespan in the wild is 11.3 years. The eggs of the Song sparrow are brown with greenish-white spots. Females lay three to five eggs per clutch, with an average incubation time of 13–15 days before hatching.
In the field, they are most easily confused with the Lincoln's sparrow and the Savannah sparrow. The former can be recognized by its shorter, grayer tail and the differently-patterned head, the brown cheeks forming a clear-cut angular patch. The Savannah sparrow has a forked tail and yellowish flecks on the face when seen up close.
Distribution and life history
Though a habitat generalist, the Song sparrow favors brushland and marshes, including salt marshes across most of Canada and the United States. They also thrive in human dominated areas such as in suburbs, agricultural fields, and along roadsides. Permanent residents of the southern half of their range, northern populations of the song sparrow migrate to the southern United States or Mexico during winter and intermingle with the native, non-migratory population. The song sparrow is a very rare vagrant to western Europe, with a few recorded in Great Britain and Norway.
These birds forage on the ground, in shrubs or in very shallow water. They mainly eat insects and seeds. Birds in salt marshes may also eat small crustaceans. They nest either in a sheltered location on the ground or in trees or shrubs. Song Sparrows with areas of shrub cover in their territory, away from the intertidal coastline, have greater over-winter survival, as well higher reproductive success.
The song sparrow has been the subject of several studies detailing the physiological reactions of bird species to conditions such as daylight length and differing climatic conditions. Most birds gain mass in their reproductive organs in response to some signal, either internal or external as the breeding season approaches. The exact source of this signal varies from species to species - for some, it is an endogenous process separate from environmental cues, while other species require extensive external signals of changing daylight length and temperature before beginning to increase the mass of their reproductive organs. Male specimens of M. melodia gain significant testicular mass in response both to changes in the daily photoperiod and as a result of endogenous chemical signals. Females also undergo significant ovarian growth in response to both photo-period and endogenous signals. In this way, M. melodia is amongst only a handful of birds that use both external and engodenous signalling to dictate their breeding season. Hormone levels in both males and females were found fluctuate throughout the breeding season, having very high levels in March and late April and then declining until May. These studies suggest that there are multiple factors at work that influence when and how the song sparrow breeds other than just increasing day length.
Due to the myriad subspecies of the song sparrow and the extremely varied climate of southern California, where many of these subspecies make their homes, physiological studies were undertaken to determine how climatic conditions and local environment influenced the bill size of M. melodia subspecies. The bill of a bird is highly important for thermoregulation as the bare surface area makes a perfect place to radiate excess heat or absorb solar energy to maintain homeostasis. Knowing this, comparisons of bill length between individual song sparrows collected in different habitats were made with regard to the primary habitat type or microclimate that they were collected in. Larger beaked subspecies were strongly correlated with hotter microclimates - a correlation that follows from the conditions of Allen's Rule.
The sparrow species derives its name from its colorful repertoire of songs. Enthusiasts report that one of the songs heard often in suburban locations closely resembles the opening four notes of Ludwig van Beethoven's Symphony No. 5. The male uses a fairly complex song to declare ownership of its territory and attract females.
Singing itself consists of a combination of repeated notes, quickly passing isolated notes, and trills. The songs are very crisp, clear, and precise, making them easily distinguishable by human ears. A particular song is determined not only by pitch and rhythm but also by the timbre of the trills. Although one bird will know many songs—as many as 20 different tunes with as many as 1000 improvised variations on the basic theme,—unlike thrushes, the song sparrow usually repeats the same song many times before switching to a different song.
Song sparrows typically learn their songs from a handful of other birds that have neighboring territories. They are most likely to learn songs that are shared between these neighbors. Ultimately, they will choose a territory close to or replacing the birds that they have learned from. This allows the song sparrows to address their neighbors with songs shared with those neighbors. It has been demonstrated that song sparrows are able to distinguish neighbors from strangers on the basis of song, and also that females are able to distinguish (and prefer) their mate's songs from those of other neighboring birds, and they prefer songs of neighboring birds to those of strangers.
Predators and parasites
Common predators of the song sparrow include cats, hawks, and owls, however snakes, dogs, and the American kestrel are treated ambiguously, suggesting that they are less of a threat. The song sparrow recognizes enemies by both instinctual and learned patterns (including cultural learning), and adjusts its future behavior based on both its own experiences in encounters, and from watching other birds interact with the enemies. Comparisons of experiments on hand-raised birds to observation of birds in the wild suggest that the fear of owls and hawks is instinctual, but fear of cats is learned.
Song sparrows' nests are parasitized by the brown-headed cowbird. The cowbirds' eggs closely resemble song sparrows' eggs, although the cowbirds' eggs are slightly larger. Song sparrows recognize cowbirds as a threat and attack the cowbirds when they are near the nest. There is some evidence that this behavior is learned rather than instinctual. A more recent study found that the behavior of attacking female cowbirds near nests may actually attract cowbird parasitism because the female cowbirds use such behavior to identify female song sparrows that are more likely to successfully raise a cowbird chick. One study found that while cowbird parasitism did result in more nest failure, overall there were negligible effects on song sparrow populations when cowbirds were introduced to an island. The study pointed to a number of explanatory factors including song sparrows raising multiple broods, and song sparrows' abilities to raise cowbird chicks with their own.
The song sparrow is one of the birds with the most numerous subspecies in North America, and even on a global scale rivals such species as the horned lark, the yellow wagtail, the golden whistler or the island thrush; 52 subspecies were named altogether, of which 24 are now considered valid. It is a cryptic species.
Small, brownish, long-winged forms with strong black streaks.
- Melospiza melodia melodia (Wilson, 1810). The nominate subspecies. Eastern half of North American range except coastal areas south from New York State. In winter, they migrate southeastwards. Very contrasting, very light with black streaks below, and gray margins to back feathers. This population includes the forms named as M. m. juddi Bishop, 1896; M. m. acadica Thayer and Bangs, 1914; M. m. beata (non Bangs) Todd, 1930; M. m. euphonia Wetmore, 1936; M. m. callima Oberholser, 1974; and M. m. melanchra Oberholser, 1974.
- Melospiza melodia atlantica Todd, 1924. Inhabits the Atlantic Coast sand dunes and salt marshes from New York State southwards. Differs from nominate by a gray back. Includes M. m. rossignolii Bailey, 1936.
- Melospiza melodia montana Henshaw, 1884. The subspecies west of melodia to the Rocky Mountains. Some birds from the northern part of its range migrate to north-west Mexico in winter. Similar to nominate, but larger, duller coloration and more slender bill. Includes M. m. fisherella Oberholser, 1911.
Large, dark, diffuse dark streaks. A study of mtDNA allozyme variation of most forms in this group concluded that they are of comparatively recent origin and that island populations are apparently derived independently from each other.
- Melospiza melodia maxima Gabrielson & Lincoln, 1951, giant song sparrow. W Aleutian Islands (Attu to Atka Island), resident. The largest subspecies, about the size of the California towhee. Very gray overall, long, diffuse streaks. Bill long and slender.
- Melospiza melodia sanaka McGregor, 1901, Aleutian song sparrow. Aleutians from Seguam Island east to Stepovak Bay, Alaska, and islands to the south of Alaskan Peninsula; resident. Similar to maxima; grayer still and bill even more slender. Includes the Semidi song sparrow, M. m. semidiensis Brooks, 1919, which may be a distinct subspecies however. Also includes the population from Amak Island named M. m. amaka Gabrielson & Lincoln, 1951 (Amak song sparrow) which was extirpated due to habitat destruction, apparently disappearing in the weeks around New Year's Eve, 1980/1981 (there were unconfirmed sightings in 1987 and 1988).
- Melospiza melodia insignis Baird, 1869, Bischoff song sparrow. Kodiak, Afognak, Sitkalidak, and Raspberry Islands, and Kukak and Katmai on Alaska Peninsula; many migrate south in winter. A darkish gray, medium-sized form.
- Melospiza melodia kenaiensis Ridgway, 1900, Kenai song sparrow. Resident; Pacific coast of Kenai Peninsula and Prince William Sound islands; some resident, some migrant. Smaller and browner than insignis.
- Melospiza melodia caurina Ridgway, 1899, Yakutat song sparrow. Northern Gulf of Alaska coast, many migrate to Pacific Northwest in winter. A smaller version of kenaiensis.
- Melospiza melodia rufina (Bonaparte, 1850), sooty song sparrow. Outer islands of Alexander Archipelago and Haida Gwaii (Queen Charlotte Islands); most are resident. A very dark, rufous, and small form. Includes M. m. kwaisa Cumming, 1933.
- Melospiza melodia morphna Oberholser, 1899. Coastal region of central British Columbia south to NW Oregon; resident. Lighter, more rufous than rufina. Previously M. m. cinerea (non Gmelin) (Audubon, 1839); M. m. phaea Fisher, 1902 are Central Oregon hybrids between this subspecies and M. m. cleonensis.
- Melospiza melodia merrilli Brewster, 1896. Occurs between the ranges of morphna and montana south to N Nevada; some migrate south in winter. Includes M. m. ingersolli McGregor, 1899 and M. m. inexspectata Riley, 1911 (Riley song sparrow; inexpectata is a common lapsus). Doubtfully distinct; intermediate between morphna and montana in appearance also and may be hybrid birds.
- Melospiza melodia cleonensis McGregor, 1899. SW Oregon west of Cascade Mountains south to NW California. Brownish-buffish, notably on the flanks; no gray on back; underside with somewhat diffuse chestnut streaks.
Cismontane California group
Small, well-marked and short-winged brownish forms. All resident, except occasional birds from upland populations.
- Melospiza melodia gouldii Baird, 1858. Coastal central California, except San Francisco Bay. A very brown and clear-marked subspecies; buffish (not light gray) fringes of upper back. M. m. santaecrucis Grinnell, 1901 are hybrids with birds from southwards and Central Valley populations.
- Melospiza melodia samuelis (Baird, 1858), San Pablo song sparrow. N San Francisco Bay and San Pablo Bay saltmarshes. A small, tiny-billed subspecies with dirty olive upperpart background.
- Melospiza melodia maxillaris Grinnell, 1909, Suisun song sparrow. Suisun Bay marshes. Dark upperparts; brown with gray mantle edges; plump bill base.
- Melospiza melodia pusillula Ridgway, 1899, Alameda song sparrow. E San Francisco Bay saltmarshes. Yellowest subspecies, paler than samuelis and clear yellow hue below.
- Melospiza melodia heermanni Baird, 1858. Central coastal California and Central Valley south to N Baja California. Similar in color to maxillaris but medium-sized mainland subspecies. Some N-S variation with birds becoming blacker on backs, local populations once separated as M. m. cooperi Ridgway, 1899 and M. m. mailliardi Grinnell, 1911. The latter, occurring around Modesto, may be distinct.
- Melospiza melodia graminea Townsend, 1890. Described from Santa Barbara Island, California Channel Islands. A smaller, pale-gray version of heermanni. Originally called Santa Barbara song sparrow; birds from the Coronado Islands were described as M. m. coronatorum Grinnell and Daggett, 1903, those from San Miguel Island as M. m. micronyx Grinnell, 1928 and those from San Clemente, Santa Rosa and Anacapa Islands as M. m. clementae Townsend, 1890. Hybrid population with heermanni on Santa Cruz Island. Extirpated on Santa Barbara (and possibly San Clemente) by feral cats, c. 1967–1970.
Small, pale, streaks rufous; all resident.
- Melospiza melodia fallax (Baird, 1854), desert song sparrow. Sonoran and parts of Mojave Deserts to E Arizona. A pale ruddy desert form. Synonyms are M. m. saltonis Grinnell, 1909, M. m. virginis Marshall and Behle, 1942 and M. m. bendirei Phillips, 1943.
- Melospiza melodia rivularis Bryant, 1888. Central Baja California. Similar to fallax, lightly streaked breast and long slender bill.
- Melospiza melodia goldmani Nelson, 1899. Not yet found outside El Salto area, Sierra Madre Oriental. Dark reddish brown back with brownish streaks just as in morphna.
Mexican Plateau group
Black-spotted, white throats; all resident.
- Melospiza melodia adusta Nelson, 1899. Río Lerma drainage from Zacapú to Lago Yuriria. Bold black pattern on belly and back, clear white throat. Birds become less ruddy brown going east.
- Melospiza melodia villai Phillips and Dickerman, 1957. Headwaters of Río Lerma near Toluca. Darker and duller brown than adusta, distinctly large.
- Melospiza melodia mexicana Ridgway, 1874. Hidalgo to Puebla. Duller and paler than adusta, birds becoming grayish going south. Includes M. m. azteca Dickerman, 1963 and M. m. niceae Dickerman, 1963. "M. m. pectoralis" (ex von Müller, 1865) cannot be assigned to a known song sparrow population.
Seen as a whole, the song sparrow is widespread and common enough to be classified as Species of Least Concern by the IUCN. The taxa mailliardi, maxillaris, samuelis (all Category 3), pusillula (Category 2), and graminea (Category 1) are listed as Species of Special Concern in California.
- BirdLife International (2012). "Melospiza melodia". IUCN Red List of Threatened Species. Version 2013.2. International Union for Conservation of Nature. Retrieved 26 November 2013.
- "eNature: Song Sparrow Melospiza melodia". Archived from the original on 2014-04-13. Retrieved 2012-04-03. Cite uses deprecated parameter
- The Cornell lab of ornithology: Song Sparrow Melospiza melodia
- CRC Handbook of Avian Body Masses by John B. Dunning Jr. (Editor). CRC Press (1992). ISBN 978-0849342585.
- Wasser, D. E.; Sherman, P. W. (2010). "Avian longevities and their interpretation under evolutionary theories of senescence". Journal of Zoology. 280 (2): 103. doi:10.1111/j.1469-7998.2009.00671.x.
- Germain, R.R.; Schuster, R.; Tarwater, C.E.; Hochachka, W.M.; Arcese, P. (2018). "Adult survival and reproductive rate are linked to habitat preference in territorial, year‐round resident Song Sparrows Melospiza melodia". Ibis. 160 (3): 568–581. doi:10.1111/ibi.12557.
- Wingfield, John C. (1993). "Control of Testicular Cycles in the Song Sparrow, Melospiza melodia melodia: Interaction of Photoperiod and an Endogenous Program?". General and Comparative Endocrinology. 92 (3): 388–401. doi:10.1006/gcen.1993.1176. PMID 8138105.
- Wingfield, John C. (1984). "Environmental and endocrine control of reproduction in the song sparrow, Melospiza melodia: I. Temporal organization of the breeding cycle". General and Comparative Endocrinology. 56 (3): 406–416. doi:10.1016/0016-6480(84)90083-2.
- Wilmer, Pat (2009). Environmental Physiology of Animals. Wiley. ISBN 9781405107242.
- Greenberg, Danner; R., R.M (2012). "The influence of the California marine layer on bill size in a generalist songbird". Evolution. 66 (12): 3825–35. doi:10.1111/j.1558-5646.2012.01726.x. PMID 23206140.
- O'Loghlen, A. L.; Beecher, M.D. (1999). "Mate, neighbour and stranger songs: a female song sparrow perspective". Animal Behaviour. 58 (1): 13–20. doi:10.1006/anbe.1999.1125. PMID 10413536.
- Nice, Margaret M.; Ter Pelkwyk & Joost (1941). "Enemy Recognition by the Song Sparrow". The Auk. 58 (2): 195–214. doi:10.2307/4079104. JSTOR 4079104.
- Smith, James N. M.; Arcese, Peter; McLean, Ian G. (1984). "Age, experience, and enemy recognition by wild song sparrows". Behavioral Ecology and Sociobiology. 14 (2): 101. doi:10.1007/BF00291901.
- Smith, James N. M. & Arcese, Peter (1994). "Brown-Headed Cowbirds and an Island Population of Song Sparrows: A 16-Year Study". The Condor. 96 (4): 916–934. doi:10.2307/1369102. JSTOR 1369102.
- Patten, M.A. (2001). The roles of habitat and signalling in speciation: Evidence from a contact zone of two Song Sparrow (Melospiza melodia) subspecies. Ph.D. diss., Univ. of California, Riverside.
- Arcese, P.; Sogge, M.K.; Marr, A.B. & Patten, M.A. (2002). "Song Sparrow (Melospiza melodia)." In: Poole, A. & Gill, F.: The Birds of North America 704. The Birds of North America, Inc., Philadelphia, PA.
- Hare, M.P. & Shields, G.F. (1992). "Mitochondrial-DNA variation in the polytypic Alaskan song sparrow" (PDF). Auk. 109 (1): 126–132. doi:10.2307/4088273. JSTOR 4088273.
- Gabrielson, Ira N. & Lincoln, Frederick C. (1951). "The Races of Song Sparrows in Alaska" (PDF). Condor. 53 (5): 250–255. doi:10.2307/1364957. JSTOR 1364957.
- Pruett, Christin; Gibson, Daniel D. & Winker, Kevin (2003 (2004). "Amak Island Song Sparrows (Melospiza melodia amaka) are not evolutionarily significant". Ornithological Science. 3 (2): 133–138. doi:10.2326/osj.3.133.CS1 maint: multiple names: authors list (link)
- California Department of Fish and Game (CDFG) (2006). California Bird Species of Special Concern.
- Beecher, M.D.; Campbell, S.E.; Stoddard, P.K. (1994). "Correlation of Song Learning and Territory Establishment Strategies in the Song Sparrow" (PDF). Proc. Natl. Acad. Sci. USA. 91 (4): 1450–1454. doi:10.1073/pnas.91.4.1450. PMC 43177. PMID 11607460.
- Stoddard, Beecher; Horning, C.L.; Campbell, S.E. (1991). "Recognition of individual neighbors by song in the song sparrow, a species with song repertoires". Behavioral Ecology and Sociobiology. 29 (3): 211–215. doi:10.1007/bf00166403.
- O'Loghlen, A.L.; Beecher (1997). "Sexual preferences for mate song types in female song sparrows" (PDF). Animal Behaviour. 53 (4): 835–841. doi:10.1006/anbe.1996.0348.
- Smith, J.N.M.; et al. (1997). "A metapopulation approach to the population biology of the Song Sparrow Melospiza melodia". Ibis. 138 (4): 120–128. doi:10.1111/j.1474-919x.1996.tb04318.x.
|Wikimedia Commons has media related to the song sparrow.|
|Wikispecies has information related to Melospiza melodia|
- Song sparrow ID, including sound and video, at Cornell Lab of Ornithology
- Song sparrow facts at BirdHouses101.com
- Song sparrow species account – Cornell Lab of Ornithology
- Song sparrow - Melospiza melodia - USGS Patuxent Bird Identification InfoCenter
- "Song sparrow media". Internet Bird Collection.
- Song sparrow photo gallery at VIREO (Drexel University)