Overview

Brief Summary

Biology

The coot feeds on pondweeds and invertebrates (4); it dives rather clumsily to obtain food, and returns to the surface rapidly thanks to its cork-like buoyancy (6). Unlike ducks, coots bring their food to the surface before eating it; this results in frequent cases of food stealing (4). They are opportunistic birds, and may feed in grasslands at certain times of the year (6). During winter, large flocks may gather on large lakes and reservoirs (10), these gatherings are relatively peaceful compared to the fierce territorial aggression seen during the breeding season (2). The nest, a mound of dead reeds, is usually built amongst emergent vegetation (6). From mid-March, between 6 and 9 speckled eggs are laid (occasionally up to 15 eggs, though these large clutches may be laid by more than one female (10)). The eggs are incubated by both parents for up to 24 days (6). The chicks leave the nest a few days after hatching, and reach independence at around 8 weeks of age (6). Two broods are produced a year, but occasionally a third brood may occur (6).
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Comprehensive Description

Description

The coot, Britain's largest rail species (4), is a plump water bird; it has a greyish body, a black head, and a white bill, above which there is a prominent white 'frontal shield' (2). The saying 'as bald as a coot' refers to this frontal plate, as do a number of local names for the species, including 'bald coot' and 'white-faced diver' (5). Juveniles have whitish areas on the sides of the head, breast and fore neck; the rest of the body is brownish-grey. The young are covered in black down and have red and blue markings on the head (2). Coots produce a variety of vocalisations, including a loud 'kowk', and a sharp 'pitts' (2).
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Distribution

Range

Widespread and common throughout Britain, but absent from hilly areas and most parts of northern and western Scotland (6). Elsewhere, it is found in Europe, northern Africa, the Middle East, through Eurasia, reaching as far east as the Pacific coast of China and Japan. It is also found in Australasia, south-east Asia, and India (8).
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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
Behaviour Most populations in warm and temperate regions are resident1, often making nomadic dispersive movements according to changing water levels and seasonal rainfall1, 4.Populations in northern Eurasia are fully migratory however, migrating on a broad front through continental Europe and across the Sahara2. Southward movements occur from mid-August to November2, with the return passage occurring from late-February2 to May1. The species nests in dispersed solitary pairs1, 3, 4, although it is largely gregarious1 with flocks (sometimes of several thousand individuals3) frequently forming during the winter2, 3, 4. Adults undergo a post-breeding flightless moult period, with flocks of moulting birds congregating from June-September1, 2, 3. The species is diurnally active and roosts at sunset solitarily or in flocks2. It may feed in flocks on land, especially when winds cause high waves on water1. Habitat The species inhabits large, still or slow-flowing waters1, 3 and shows a preference for shallow water with adjacent deeper water (e.g. > 2 m) for diving2, and muddy substrates, marginal, emergent, floating or submergent vegetation1, 2, 3. Habitats include eutrophic and mesotrophic2 lakes1, 3, pools, ponds, reservoirs, barrages, gravel-pits, canals, drainage ditches, dykes, oxbow lakes1, 2, 3, fish ponds7, creeks1, 2, rivers1 and river deltas2, as well as open marshes1, 2, freshwater meadows2, flood-lands1, 2, 3, freshwater and saline lagoons4, salt-pans, clay-pans1, 2 and sewage ponds2. It frequently exploits temporary pools and seasonally inundated marshes when breeding (Africa)4, and may extend to quiet estuaries or inshore waters in the winter1. It generally avoids closely overgrown, narrowly confined and very shallow waters, and those overshadowed by trees or cliffs2. If solitary the species roosts at sunset on small islets, mudbanks, sandbanks, rocks in water, floating mats of vegetation, floating logs, or branches of trees over water, preferring to roost on open water, in shore vegetation or in meadows adjacent to water if in flocks2. Diet This species is omnivorous, although its diet consists primarily of vegetable matter1 such as algae (e.g. Chara, Cladophora, Spirogyra), the vegetative pasts of aquatic and terrestrial plants (e.g. waterweeds, bulrushes, reeds and grasses), the seeds of waterweeds, sedges, water-lilies, grasses and cereal crops1, clubmoss Selaginella and aquatic fungi (e.g. Leptomitus)2. Animal matter in its diet includes molluscs, adult and larval insects (especially flies, caddisflies, Odonata, Lepidoptera, beetles and bugs)1, 2, worms, leeches, shrimps, spiders1, small fish1, 4, fish eggs, frogs, birds and bird eggs, and small mammals1. Breeding site The nest is a platform of vegetation that may be resting on the bottom of shallow water, floating or on a foundation of trampled plant matter in emergent vegetation1. The species may also nest on artificial platforms, islands, rafts, tree stumps, tree forks1 or in bushes up to 3 m above the water2. Management information A study in the Czech Republic found that fish ponds with a fish stock density of less than 400 kg/ha, water transparency of more than 50 cm, mixed fish stocks (e.g. tench and pike or perch) rather than monospecific stocks (e.g. of carp), and systems that include ponds with fish fry (to provide areas with low fish competition and high invertebrate availability) are more successful in supporting breeding pairs of this species7. The cyclical removal of adult fish from an artificial waterbody (gravel pit) in the UK (leaving small fish for piscivorous birds) resulted in increased winter use of the habitat by the species as result of an increase in the growth of submerged aquatic macrophytes15. The removed fish (dead or alive) were sold to generate funds15.

Systems
  • Terrestrial
  • Freshwater
  • Marine
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Depth range based on 4 specimens in 2 taxa.
Water temperature and chemistry ranges based on 3 samples.

Environmental ranges
  Depth range (m): 0 - 0
  Temperature range (°C): 9.758 - 10.336
  Nitrate (umol/L): 3.256 - 10.807
  Salinity (PPS): 32.945 - 33.882
  Oxygen (ml/l): 6.553 - 6.579
  Phosphate (umol/l): 0.345 - 0.640
  Silicate (umol/l): 2.505 - 7.273

Graphical representation

Temperature range (°C): 9.758 - 10.336

Nitrate (umol/L): 3.256 - 10.807

Salinity (PPS): 32.945 - 33.882

Oxygen (ml/l): 6.553 - 6.579

Phosphate (umol/l): 0.345 - 0.640

Silicate (umol/l): 2.505 - 7.273
 
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Habitat

Found in most shallow, still or slow-moving freshwater habitats including ponds, lakes, rivers, marshes, gravel pits and reservoirs (6).
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Associations

Known prey organisms

Fulica atra (pochard, swan, coot) preys on:
Potamogeton
Phragmites

Based on studies in:
Scotland (Lake or pond)

This list may not be complete but is based on published studies.
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Associations

In Great Britain and/or Ireland:
Animal / parasite / endoparasite
fluke of Cyclocoelum mutabile endoparasitises lung of Fulica atra

Animal / parasite / endoparasite
fluke of Dendritobilharzia pulverulenta endoparasitises renal vein of Fulica atra

Animal / parasite / endoparasite
fluke of Diorchis endoparasitises small intestine of Fulica atra

Animal / parasite / endoparasite
Diorchis inflata endoparasitises small intestine of Fulica atra

Animal / parasite / endoparasite
adult of Diplostomum endoparasitises intestine of Fulica atra

Animal / parasite / endoparasite
fluke of Eucotyle endoparasitises kidney of Fulica atra

Animal / parasite / endoparasite
fluke of Filicollis anatis endoparasitises small intestine of Fulica atra

Animal / parasite / endoparasite
fluke of Notocotylus gibbus endoparasitises caecum of Fulica atra

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Life History and Behavior

Life Expectancy

Lifespan, longevity, and ageing

Maximum longevity: 20.6 years (wild) Observations: Record longevity may be underestimated (John Terres 1980).
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Molecular Biology and Genetics

Molecular Biology

Barcode data: Fulica atra

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

 
There are 6 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.
 
BON186-07|NHMO-BC186|Fulica atra| ------------------------CACAAAGACATTGGCACACTCTACTTAATTTTCGGAGCCTGAGCCGGCATAATCGGCACCGCCCTC---AGCCTGCTTATCCGAGCAGAATTAGGACAACCCGGCACCCTCCTAGGAGAT---GACCAAATTTACAACGTAATCGTCACCGCCCACGCCTTTGTAATAATTTTCTTTATAGTAATACCAATCATAATCGGAGGCTTCGGCAACTGACTAGTACCCCTCATA---ATCGGAGCCCCAGACATAGCATTTCCCCGCATAAATAACATAAGCTTCTGACTCCTTCCTCCCTCCTTCCTACTACTCTTAGCATCATCCACAGTAGAAGCAGGAGCAGGCACAGGATGAACAGTTTACCCCCCACTAGCCGGCAACCTAGCACATGCAGGCGCTTCAGTTGACCTA---GCCATCTTCTCCCTCCACTTAGCAGGTGTCTCATCTATTCTAGGCGCCATCAATTTTATTACAACTGCCATCAACATAAAACCACCCGCCCTATCCCAATATCAAACTCCTCTGTTCGTATGATCTGTCCTCATTACCGCTGTTCTACTACTGCTATCCCTCCCTGTCCTTGCCGCT---GGCATTACCATACTACTAACCGACCGAAACCTAAATACCACATTCTTCGACCCAGCCGGAGGAGGTGATCCCATCCTATACCAACACCTCTTCTGATTTTTCGGACACCCAGAAGTCTATATCCTAATCCTCCCTGGATTCGGAATC---------------------------------------------------------------------------------------------------------------------------------------- 
-- end --

Download FASTA File
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Statistics of barcoding coverage: Fulica atra

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 6
Species: 8
Species With Barcodes: 1

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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
LC
Least Concern

Red List Criteria

Version
3.1

Year Assessed
2009

Assessor/s
BirdLife International

Reviewer/s
Bird, J., Butchart, S.

Contributor/s

Justification
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.

History
  • 2008
    Least Concern
  • 2004
    Least Concern
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Status in Egypt

Regular passage visitor and winter visitor.

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IUCN

Least Concern.

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Status

Receives general protection under the Wildlife and Countryside Act, 1981 (3). Included in the Birds of Conservation Concern Green List (low conservation concern) (9).
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Population

Population
Total regarded as a minimum by Wetlands International (2006).
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Threats

Threats

Major Threats
This species suffers disturbance10 and mortality (Azerbaijan) from hunting1, and is poisoned by ingesting lead shot (France)11. It is also threatened by oil and petroleum pollution (Azerbaijan1 and the Kaliningrad region, Russia5), and by habitat degradation and loss due to agricultural drainage schemes (Pakistan)2, wetland drainage, peat-extraction, changing wetland management practices (decreased grazing and mowing in meadows leading to scrub over-growth) and the burning and mowing of reeds5. The species is often drowned in freshwater fishing nets with mesh sizes greater than 5 cm (China)12, and suffers predation from American mink Neovison vison (Slonsk Reserve, Poland13 and UK14). It is also susceptible to avian influenza, so may be threatened by future outbreaks of the virus6. Utilisation The species is hunted for sport in the Mediterranean2, Denmark9, Northern Ireland10 and Iran8, and for food in the Mediterranean2, Iran8, India, Pakistan, Afghanistan and neighbouring countries2, especially when it is flightless during the post-breeding moult2.
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Threats

This species is not threatened; in fact the population has increased somewhat since the 1970s (7).
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Management

Conservation

The coot receives general protection in Britain under the Wildlife and Countryside Act, 1981. A number of populations occur in Special Protection Areas (8).
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Wikipedia

Eurasian Coot

The Eurasian Coot, Fulica atra, also known as Coot, is a member of the rail and crake bird family, the Rallidae. The Australian subspecies is known as the Australian Coot.

Contents

Distribution

The Coot breeds across much of the Old World on freshwater lakes and ponds. It occurs and breeds in Europe, Asia, Australia, and Africa. The species has recently expanded its range into New Zealand. It is resident in the milder parts of its range, but migrates further south and west from much of Asia in winter as the waters freeze.

Description

The Coot is 32–42 cm (13–17 in) long and weighs 585–1,100 g (1.29–2.4 lb), and is largely black except for the white facial shield (which gave rise to the phrase "as bald as a coot", which the Oxford English Dictionary cites in use as early as 1430).[3] As a swimming species, the Coot has partial webbing on its long strong toes.

The juvenile is paler than the adult, has a whitish breast, and lacks the facial shield; the adult black plumage develops when about 3–4 months old, but the white shield is only fully developed at about one year old.

This is a noisy bird with a wide repertoire of crackling, explosive, or trumpeting calls, often given at night.

Behaviour

Adult with a pair of juveniles

The Coot is much less secretive than most of the rail family, and can be seen swimming on open water or walking across waterside grasslands. It is an aggressive species, and strongly territorial during the breeding season, and both parents are involved in territorial defence.[4] During the non-breeding season they may form large flocks, possibly related to predator avoidance.[5]

It is reluctant to fly and when taking off runs across the water surface with much splashing. They do the same, but without actually flying, when travelling a short distance at speed in territorial disputes. As with many rails, its weak flight does not inspire confidence, but on migration, usually at night, it can cover surprisingly large distances. It bobs its head as it swims, and makes short dives from a little jump.

Breeding

Young chick in Australia

This species builds a nest of dead reeds or grasses, but also pieces of paper or plastic near the water's edge or on underwater obstacles protruding from the water, laying up to 10 eggs, sometimes 2 or 3 times per season. Usually only a few young survive. They are frequent prey for birds such as herons and gulls.

Coots can be very brutal to their own young under pressure such as the lack of food. They will bite young that are begging for food and repeatedly do this until it stops begging and starves to death. If the begging continues, they may bite so hard that the chick is killed.[6]

Diet

The Coot is an omnivore, and will take a variety of small live prey including the eggs of other water birds, as well as algae, vegetation, seeds and fruit.[7] It shows considerable variation in its feeding techniques, grazing on land or in the water. In the water it may upend in the fashion of a Mallard or dive in search of food.[8]

Status

The Eurasian Coot is one of the species to which the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) applies.

Gallery

References

  1. ^ BirdLife International (2004). Fulica atra. 2006. IUCN Red List of Threatened Species. IUCN 2006. www.iucnredlist.org. Retrieved on 10 May 2006. Database entry includes justification for why this species is of least concern.
  2. ^ Condon, H. T. (1975) Checklist of the Birds of Australia: Non-Passerines Royal Australasian Ornithologists Union, 57:311
  3. ^ CRC Handbook of Avian Body Masses by John B. Dunning Jr. (Editor). CRC Press (1992), ISBN 978-0-8493-4258-5.
  4. ^ Cave,A.J.; J.Visser; A.C. Perdeck. (1989). "Size and quality of the Coot (Fulica atra) territory in relation to age of its tenants and neighbours". Ardea 77: 87 - 97
  5. ^ van den Hout PJ (2006) "Dense foraging flotillas of Eurasian coots Fulica atra explained by predation by Ganges soft-shell turtle Aspideretus gangeticus?". Ardea 94 (2): 271-274
  6. ^ Attenborough, David (1998 Episode 9, 12 mins ff.). The Life of Birds. Princeton: Princeton University Press. ISBN 978-0-691-01633-7. 
  7. ^ Martin R. Perrow, J. Hans Schutten, John R. Howes, Tim Holzer, F. Jane Madgwick and Adrian J. D. Jowitt (1997) "Interactions between coot (Fulica atra) and submerged macrophytes: the role of birds in the restoration process". Hydrobiologia 342/343: 241–255 doi:10.1023/A:1017007911190
  8. ^ Brigitte J. Bakker and Robin A. Fordham (1993) "Diving behaviour of the Australian Coot in a New Zealand lake". Notornis 40 (2): 131–136
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