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Brief Summary

House martins like to nest against steep rocks. Although the Netherlands doesn't have much natural rock, house martins are very content here. Instead of rocky walls, they build their nests against houses. They make a ball from clay under the eaves, with the opening on the top. House martins often live in colonies. There can be dozens together during a good year. After nesting, all of the house martins migrate to Africa, returning again in April or May.
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© Copyright Ecomare

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Habitat and Ecology

  • Terrestrial
  • Freshwater
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© International Union for Conservation of Nature and Natural Resources

Source: IUCN


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Depth range based on 15 specimens in 1 taxon.
Water temperature and chemistry ranges based on 12 samples.

Environmental ranges
  Depth range (m): 0 - 0
  Temperature range (°C): 9.458 - 12.984
  Nitrate (umol/L): 2.286 - 12.040
  Salinity (PPS): 31.635 - 35.345
  Oxygen (ml/l): 6.114 - 6.746
  Phosphate (umol/l): 0.273 - 0.653
  Silicate (umol/l): 1.963 - 7.673

Graphical representation

Temperature range (°C): 9.458 - 12.984

Nitrate (umol/L): 2.286 - 12.040

Salinity (PPS): 31.635 - 35.345

Oxygen (ml/l): 6.114 - 6.746

Phosphate (umol/l): 0.273 - 0.653

Silicate (umol/l): 1.963 - 7.673
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.


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In Great Britain and/or Ireland:
Animal / guest
puparium of Crataerina hirundinis is a guest in nest of Delichon urbica
Other: major host/prey

Animal / associate
larva of Fannia parva is associated with nest of Delichon urbica

Animal / associate
larva of Fannia rondanii is associated with nest of Delichon urbica

Animal / parasite / ectoparasite / blood sucker
adult of Oeciacus hirundinis sucks the blood of nestling of Delichon urbica
Other: major host/prey


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Life History and Behavior

Life Expectancy

Lifespan, longevity, and ageing

Maximum longevity: 14.5 years (wild)
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© Joao Pedro de Magalhaes

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Molecular Biology and Genetics

Molecular Biology

Barcode data: Delichon urbicum

The following is a representative barcode sequence, the centroid of all available sequences for this species.

There are 10 barcode sequences available from BOLD and GenBank.

Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.

See the BOLD taxonomy browser for more complete information about this specimen and other sequences.

-- end --

Download FASTA File

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Statistics of barcoding coverage: Delichon urbicum

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 10
Specimens with Barcodes: 14
Species With Barcodes: 1
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Conservation Status

IUCN Red List Assessment

Red List Category
Least Concern

Red List Criteria


Year Assessed

BirdLife International

Butchart, S. & Symes, A.


This species has an extremely large range, and hence does not approach the thresholds for Vulnerable under the range size criterion (Extent of Occurrence <20,000 km2 combined with a declining or fluctuating range size, habitat extent/quality, or population size and a small number of locations or severe fragmentation). Despite the fact that the population trend appears to be decreasing, the decline is not believed to be sufficiently rapid to approach the thresholds for Vulnerable under the population trend criterion (>30% decline over ten years or three generations). The population size is extremely large, and hence does not approach the thresholds for Vulnerable under the population size criterion (<10,000 mature individuals with a continuing decline estimated to be >10% in ten years or three generations, or with a specified population structure). For these reasons the species is evaluated as Least Concern.
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Status in Egypt

Regular passage visitor, non-breeding summer visitor? and winter visitor?

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© Bibliotheca Alexandrina

Source: Bibliotheca Alexandrina - EOL Ar


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In Europe, the breeding population is estimated to number 9,900,000-24,000,000 breeding pairs, equating to 29,700,000-72,000,000 individuals (BirdLife International 2004). Europe forms 25-49% of the global range, so a very preliminary estimate of the global population size is 60,600,000-288,000,000 individuals, although further validation of this estimate is needed. The population in China has been estimated at c.100-10,000 breeding pairs, c.50-1,000 individuals on migration and < c.50 wintering individuals (Brazil 2009).

Population Trend
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Common house martin

The common house martin (Delichon urbicum), sometimes called the northern house martin or, particularly in Europe, just house martin, is a migratory passerine bird of the swallow family which breeds in Europe, north Africa and temperate Asia; and winters in sub-Saharan Africa and tropical Asia. It feeds on insects which are caught in flight, and it migrates to climates where flying insects are plentiful. It has a blue head and upperparts, white rump and pure white underparts, and is found in both open country and near human habitation. It is similar in appearance to the two other martin species of the genus Delichon, which are both endemic to eastern and southern Asia. It has two accepted subspecies.

Both the scientific and colloquial name of the bird are related to its use of human-made structures. It builds a closed cup nest from mud pellets under eaves or similar locations on buildings usually in colonies.

It is hunted by the Eurasian hobby (Falco subbuteo), and like other birds is affected by internal parasites and external fleas and mites, although its large range and population mean that it is not threatened globally. Its proximity to humans has resulted in some cultural and literary references.


The common house martin was first described by Linnaeus in his Systema Naturae in 1758 as Hirundo urbica,[3] but was placed in its current genus, Delichon, by Thomas Horsfield and Frederic Moore in 1854.[4] Delichon is an anagram of the Ancient Greek term χελιδών (chelīdōn), meaning "swallow",[5] and the species name urbicum (urbica until 2004, due to a misunderstanding of Latin grammar) means "of the town" in Latin.[6]

The genus Delichon is a recent divergence from the barn swallow genus Hirundo, and its three members are similar in appearance with blue upperparts, a contrasting white-rump, and whitish underparts. In the past, the common house martin was sometimes considered to be conspecific with the Asian house martin (D. dasypus), which breeds in the mountains of central and eastern Asia and winters in Southeast Asia, and it also closely resembles the Nepal house martin (D. nipalense), a resident in the mountains of southern Asia. Although the three Delichon martins are similar in appearance, only D. urbicum has a pure white rump and underparts.[7]

The common house martin has two geographical subspecies, the western nominate subspecies D. u. urbicum, and the eastern D. u. lagopodum, which was described by German zoologist Peter Simon Pallas in 1811. Other races, like meridionalis from around the Mediterranean have been described, but the claimed differences from the nominate race are clinal, and therefore probably invalid.[7]


The adult common house martin of the western nominate race is 13 centimetres (5.1 in) long, with a wing span of 26–29 centimetres (10.2–11.4 in) and a weight averaging 18.3 grammes (0.65 oz). It is steel-blue above with a white rump, and white underparts, including the underwings; even its short legs have white downy feathering. It has brown eyes and a small black bill, and its toes and exposed parts of the legs are pink. The sexes are similar, but the juvenile bird is sooty black, and some of its wing coverts and quills have white tips and edgings. D. u. lagopodum differs from the nominate race in that its white rump extends much further onto the tail, and the fork of its tail is intermediate in depth between that of D. u. urbicum and that of the Asian house martin.[7]

The white rump and underparts of the common house martin, very noticeable in flight, prevent confusion with other widespread Palaeoarctic swallows such as the barn swallow (Hirundo rustica), sand martin (Riparia riparia) or red-rumped swallow (Cecropis daurica). In Africa, confusion with grey-rumped swallow (Pseudhirundo griseopyga) is possible, but that species has a grey rump, off-white underparts and long, deeply forked tail.[7] The common house martin flies with a wing beat averaging 5.3 beats per second, which is faster than the wing beat of 4.4 beats per second for the barn swallow,[8] but the flight speed of 11 m·s−1 (36 ft·s−1) is typical for hirundines.[9]

The common house martin is a noisy species, especially at its breeding colonies. The male's song, given throughout the year, is a soft twitter of melodious chirps. The contact call, also given on the wintering grounds, is a hard chirrrp, and the alarm is a shrill tseep.[1][10]

Distribution and habitat[edit]

At an official bird ringing station

The subspecies D. u. urbicum breeds across temperate Eurasia east to central Mongolia and the Yenisei River, and in Morocco, Tunisia and northern Algeria,[1] and migrates on a broad front to winter in sub-Saharan Africa. D. u. lagopodum breeds eastwards of the Yenisei to Kolyma and south to northern Mongolia and northern China; it winters in southern China and Southeast Asia.[7]

The preferred habitat of the common house martin is open country with low vegetation, such as pasture, meadows and farmland, and preferably near water, although it is also found in mountains up to at least 2,200 metres (7,200 ft) altitude.[1] It is much more urban than the barn swallow, and will nest even in city centres if the air is clean enough.[1] It is more likely to be found near trees than other Eurasian swallows, since they provide insect food and also roosting sites. This species does not normally use the reed-bed roosts favoured by migrating barn swallows.[11][12]

It uses similar open habitats on the wintering grounds, but the common house martin is less conspicuous than wintering barn swallows, tending to fly higher and be more nomadic. In the tropical parts of its wintering range, like East Africa and Thailand, it appears to be mainly found in the higher areas.[7][13][14]

The common house martin is a migrant which moves on a broad-front (i.e. European birds are not funnelled through the short sea crossings used by large soaring birds, but cross the Mediterranean and Sahara).[15] While migrating they feed in the air on insects, and they usually travel in daylight.[7] Migration brings its own hazards; in 1974, several hundred thousand birds of this species were found dead or dying in the Swiss Alps and surrounding areas, caught by heavy snowfall and low temperatures. Adult survival on autumn migration depends mainly on temperature, with precipitation another major factor, but for juveniles low temperatures during the breeding season are more critical.[16] It is anticipated that since extreme weather is predicted to become more frequent with climate change, future survival rates will depend more on adverse weather conditions than at present.[16]

The common house martin returns to the breeding grounds a few days after the first barn swallows; like that species, particularly when the weather is poor, it seldom goes straight to the nesting sites, but hunts for food over large fresh water bodies.[17] There are records of migrant house martins staying to breed in Namibia and South Africa instead of returning north.[10] As would be expected for a long distance migrant, it has occurred as a vagrant eastwards to Alaska and west to Newfoundland, Bermuda and the Azores.[7][18]



A mother flying back to a full nest in the eaves of a house in Kent, England
Collecting mud for nests in Denmark
Delichon urbicumMHNT

The common house martin was originally a cliff and cave nester, and some cliff-nesting colonies still exist, with the nests built below an overhanging rock. It now largely uses human structures such as bridges and houses. Unlike the barn swallow, it uses the outside of inhabited buildings, rather than the inside of barns or stables. The nests are built at the junction of a vertical surface and an overhang, such as on house eaves, so that they may be strengthened by attachment to both planes.[7]

Breeding birds return to Europe between April and May, and nest building starts between late March in North Africa and mid-June in Lapland. The nest is a neat closed convex cup fixed below a suitable ledge, with a narrow opening at the top. It is constructed by both sexes with mud pellets collected in their beaks, and lined with grasses, hair or other soft materials. The mud, added in successive layers, is collected from ponds, streams or puddles.[7] House sparrows frequently attempt to take over the nest during construction, with the house martins rebuilding elsewhere if they are successful. The entrance at the top of the cup is so small once it is complete that sparrows cannot take over the nest.[17]

The common house martin tends to breed colonially, and nests may be built in contact with each other. A colony size of less than 10 nests is typical, but there are records of colonies with thousands of nests. Four or five white eggs are usually laid, which average 1.9 x 1.33 centimetres (0.75 x 0.52 in) in size, and weigh 1.7 grammes (0.06 oz). The female does most of the incubation, which normally lasts 14–16 days. The newly hatched chicks are altricial, and after a further 22–32 days, depending on weather, the chicks leave the nest. The fledged young stay with, and are fed by, the parents for about a week after leaving the nest. Occasionally, first-year birds from the first brood will assist in feeding the second brood.[7]

There are normally two broods each year, the nest being reused for the second brood, and repaired and used again in subsequent years. Hatching success is 90%, and fledging survival 60–80%. Third broods are not uncommon, though late nestlings are often left to starve. The average annual mortality for adults nesting in the Western Palaearctic is 40–60%, with most deaths outside the breeding season.[7] A study of British breeders gave an average adult survival rate of just under 40%, but ranging from 25% to 70%. Rainfall in the African wintering grounds is a major factor in adult survival, although wet weather in the breeding areas has very little effect.[19] Although individuals aged 10 and 14 years have been recorded, most survive less than five years.[7] For weeks after leaving the nest the young congregate in ever-increasing flocks which, as the season advances, may be seen gathering in trees or on housetops, or on the wires with swallows. By the end of October, most martins have left their breeding areas in western and central Europe, though late birds in November and December are not uncommon, and further south migration finishes later anyway.[7]

Once established, pairs remain together to breed for life; however, extra-pair copulations are common, making this species genetically polygamous, despite being socially monogamous. A Scottish study showed that 15% of nestlings were not related to their putative fathers, and 32% of broods contained at least one extra-pair chick. Extra-pair males, usually from nests where laying had already taken place, were often seen to enter other nests. The paired male initially ensured that his female spent little time alone at the nest, and accompanied her on flights, but the mate-guarding slackened after egg laying began, so the youngest nestling was the most likely to have a different father.[20]

The common house martin has been regularly recorded as hybridising with the barn swallow, this being one of the most common passerine interspecific crosses.[21] The frequency of this hybrid has led to suggestions that Delichon is not sufficiently separated genetically from Hirundo to be considered a separate genus.[7]


Nest with chicks

The common house martin is similar in habits to other aerial insectivores, including other swallows and martins and the unrelated swifts, and catches insects in flight.[7] In the breeding areas, flies and aphids make up much of the diet, and in Europe, the house martin takes a larger proportion of aphids and small flies than the barn swallow.[7] As with that species, hymenopterans, especially flying ants, are important food items in the wintering area.[7]

This species hunts at an average height of 21 metres (70 ft) during the breeding season, but lower in wet conditions.[7] The hunting grounds are typically within 450 metres (1,500 ft) of the nest, with a preference for open ground or water, the latter especially in poor weather, but the martins will also follow the plough or large animals to catch disturbed insects. On the wintering grounds, hunting takes place at a greater height of over 50 metres (165 ft).[7]

Predators and parasites[edit]

Although the common house martin is hunted by the hobby (Falco subbuteo), its aerial skills enable it to evade most predators.[11]

It is parasitised externally by fleas and mites, including the "house martin flea", Ceratophyllus hirundinis,[22] and internally by endoparasites such as Haemoproteus prognei (avian malaria), which are transmitted by blood-sucking insects including mosquitoes.[23] A Polish study showed that nests typically contained more than 29 specimens of ectoparasite, with C. hirundinis and Oeciacus hirundinis the most abundant.[24]

Conservation status[edit]

Nest with board to prevent fouling below

The common house martin has a large range, with an estimated global extent of 10 million square kilometres.[25] Its European population is estimated to be 20–48 million individuals. Global population trends have not been quantified, although there is evidence of population fluctuations.[1][7] For these reasons, the species is evaluated as Least Concern on the IUCN Red List,[2] and has no special status under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) which regulates international trade in specimens of wild animals and plants. In Europe and Britain however, population numbers indicate a declining trend,[5] and leading conservation groups in Britain have updated the conservations status to amber indicating medium conservation concern there.[26][27]

This is a species which has greatly benefited historically from forest clearance creating the open habitats it prefers, and from human habitation which has given it an abundance of safe nest sites.[7] However, populations can fluctuate locally for a number of reasons.[7] New housing has created more nest sites, and clean-air legislation has enabled breeding in the centre of major cities like London.[7] The population of house martins in Sheffield, central UK, has been estimated at 12,353 individuals.[28] Conversely, poor weather, poisoning by agricultural pesticides, lack of mud for nest building and competition with house sparrows can reduce numbers.[7] Widespread declines in common house martin numbers have been reported from central and northern Europe since 1970.[29] As an attractive bird which feeds on flying insects, the house martin has usually been tolerated by humans when it shares their buildings for nesting, although the accumulation of droppings below breeding birds can be a nuisance leading to some destruction of nests.[7]

In literature and culture[edit]

Coat of arms of Richard II featuring five martlets

This species lacks the wealth of literary references associated with its relative, the barn swallow, although it is possible that some of the older mentions for that bird might equally well refer to the house martin.[30] William Shakespeare was clearly describing the house martin when Banquo brings the nests and birds to the attention of Duncan at Macbeth's castle, Inverness:

"This guest of summer,

The temple-haunting martlet, does approve
By his loved mansionry that the heaven's breath
Smells wooingly here. No jutty, frieze,
Buttress, nor coign of vantage, but this bird
Hath made his pendant bed and procreant cradle;
Where they most breed and haunt, I have observed

The air is delicate." (Macbeth, Act I, scene VI).[30]

There are old legends, with no basis in fact, that house martins would wall-up house sparrows by closing the entrance of the mud nest with the intruder inside, or that they would gather en masse to kill a sparrow.[30]

The martlet, often believed to refer to the house martin, or possibly a swallow, was a heraldic bird with short tufts of feathers in the place of legs.[31] It was the cadency mark of the fourth son of a noble family, and features in many coats of arms, including the Plantagenets.[32] The lack of feet signified its inability to land, which explained its link to a younger son, also landless. It also represented swiftness.[30][32][33]


  1. ^ a b c d e f Snow, David; Perrins, Christopher M., eds. (1998). The Birds of the Western Palearctic concise edition (2 volumes). Oxford: Oxford University Press. pp. 1066–1069. ISBN 0-19-854099-X. 
  2. ^ a b BirdLife International (2012). "Delichon urbicum". IUCN Red List of Threatened Species. Version 2013.2. International Union for Conservation of Nature. Retrieved 26 November 2013. 
  3. ^ Linnaeus, C (1758). Systema naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I. Editio decima, reformata. (in Latin). Holmiae. (Laurentii Salvii). p. 192. H. rectricibus immaculatis, dorso nîgro-caerulescente 
  4. ^ "ITIS Standard Report Page: Delichon". The Integrated Taxonomic Information System (ITIS). Retrieved 23 January 2008. 
  5. ^ a b "House Martin Delichon urbicum (Linnaeus, 1758)". Bird facts. British Trust for Ornithology. Retrieved 24 January 2008. 
  6. ^ Sangster, George; Collinson, J. Martin; Helbig, Andreas J; Knox, Alan G; Parkin, David T. (2004). "Taxonomic recommendations for British birds: second report". Ibis 146: 153–157. doi:10.1111/j.1474-919X.2004.00268.x. 
  7. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z Turner, Angela K; Rose, Chris (1989). Swallows & Martins: an identification guide and handbook. Boston, Massachusetts, US: Houghton Mifflin. pp. 226–233. ISBN 0-395-51174-7. 
  8. ^ Liechti, Felix; Bruderer, Lukas (2002). "Wingbeat frequency of barn swallows and house martins: a comparison between free flight and wind tunnel experiments". The Journal of Experimental Biology 205 (16): 2461–2467. PMID 12124369. 
  9. ^ Bruderer, Bruno; Boldt, Andreas (2001). "Flight characteristics of birds: 1. radar measurements of speeds". Ibis 143 (2): 178–204. doi:10.1111/j.1474-919X.2001.tb04475.x. 
  10. ^ a b Sinclair, Ian; Hockey, Phil; Tarboton, Warwick (2002). SASOL Birds of Southern Africa. Struik. p. 296. ISBN 1-86872-721-1. 
  11. ^ a b Mullarney, Killian; Svensson, Lars; Zetterstrom, Dan; Grant, Peter (1999). Collins Bird Guide. Collins. p. 242. ISBN 0-00-219728-6. 
  12. ^ Pilastro, Andrea. "The Euring swallow project in Italy". Euring Newsletter – Volume 2, December 1998. Euring. 
  13. ^ Lekagul, Boonsong; Round, Philip (1991). A Guide to the Birds of Thailand. Saha Karn Baet. p. 236. ISBN 974-85673-6-2. 
  14. ^ Robson, Craig (2004). A Field Guide to the Birds of Thailand. New Holland Press. p. 206. ISBN 1-84330-921-1. 
  15. ^ Gordo, Oscar; Brotons, Lluís; Ferrer, Xavier; Comas, Pere (2005). "Do changes in climate patterns in wintering areas affect the timing of the spring arrival of trans-Saharan migrant birds?". Global Change Biology 11 (1): 12–21. doi:10.1111/j.1365-2486.2004.00875.x. 
  16. ^ a b Stokke, Bård G; Møller, Anders Pape; Sæther, Bernt-Erik; Rheinwald, Goetz; Gutscher, Hans (2005). "Weather in the breeding area and during migration affects the demography of a small long-distance passerine migrant". The Auk 122 (2): 637–647. doi:10.1642/0004-8038(2005)122[0637:WITBAA]2.0.CO;2. ISSN 0004-8038. 
  17. ^ a b Coward, Thomas Alfred (1930). The Birds of the British Isles and Their Eggs (two volumes) 2 (Third ed.). Frederick Warne. pp. 252–254. 
  18. ^ Sibley, David (2000). The North American Bird Guide. Pica Press. p. 322. ISBN 1-873403-98-4. 
  19. ^ Robinson, Robert A.; Balmer, Dawn E.; Marchant, John H. (2008). "Survival rates of hirundines in relation to British and African rainfall". Ringing and Migration 24: 1–6. doi:10.1080/03078698.2008.9674375. 
  20. ^ Riley, Helen T.; Bryant, David M.; Carter, Royston E.; Parkin, David T. (February 1995). "Extra-pair fertilizations and paternity defence in house martins, Delichon urbica". Animal Behaviour 49 (2): 495–509. doi:10.1006/anbe.1995.0065. 
  21. ^ Møller, Anders Pape (1994). Sexual Selection and the Barn Swallow. Oxford: Oxford University Press. p. 245. ISBN 0-19-854028-0. 
  22. ^ "The housemartin flea". Distribution of British fleas. Natural History Museum. Retrieved 23 January 2008. 
  23. ^ Marzal, Alfonso; de Lope, Florentino; Navarro, Carlos; Møller, Anders Pape (2005). "Malarial parasites decrease reproductive success: an experimental study in a passerine bird". Oecologia 142 (4): 541–545. doi:10.1007/s00442-004-1757-2. PMID 15688214. 
  24. ^ Kaczmarek, S. (1993). "Ectoparasites from nests of swallows Delichon urbica and Hirundo rustica collected in autumn". Wiad Parazytol. (in Polish) 39 (4): 407–409. PMID 8128730. 
  25. ^ "Northern House-martin – BirdLife Species Factsheet". BirdLife International. Retrieved 15 November 2007. 
  26. ^ "The population status of birds in the UK: Birds of Conservation Concern: 2002–2007". British Trust for Ornithology. Retrieved 28 January 2008. 
  27. ^ "House Martin". British Trust for Ornithology. Retrieved 28 January 2008. 
  28. ^ Fuller R. A., Tratalos J., Gaston K. J. (2009). "How many birds are there in a city of half a million people?". Diversity and Distributions 15 (2): 328–337. doi:10.1111/j.1472-4642.2008.00537.x. 
  29. ^ "Population trends". House Martin. Royal Society for the Protection of Birds. Retrieved 18 December 2007. 
  30. ^ a b c d Cocker, Mark; Mabey, Richard (2005). Birds Britannica. Chatto & Windus. pp. 318–319. ISBN 0-7011-6907-9. 
  31. ^ Shakespeare, William (1990). The Tragedy of Macbeth. Brooke, Nicholas (annotator). Oxford University Press. p. 115. ISBN 0-19-283417-7. 
  32. ^ a b "Curiosity Corner". Retrieved 27 January 2008. 
  33. ^ Cooper, J. C. (1992). Symbolic and Mythological Animals. London: Aquarian Press. p. 158. ISBN 1-85538-118-4. 
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