Overview

Comprehensive Description

Description

Fairly large, dark goose. Bill typically shows extensive orange, and legs are also bright orange (duller in young birds).

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Physical Description

Size

Size

Length: 70 - 90 cm.

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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
Behaviour This species is strongly migratory and travels between breeding grounds in the high Arctic to wintering grounds in the temperate and subtropical zones1. Populations that breed in the taiga nest in early-May, with those breeding in the tundra nesting one month later in early-June1, 2. The species breeds in solitary pairs, usually with nests well-dispersed6 (although it will also nest in loose groups)1. After breeding the species undergoes a moulting period when it is flightless for c.1 month between July and August5, some populations undertaking extensive northward moult migrations2, and most congregating into large moulting flocks near open water5. The species departs from its breeding grounds after this post-breeding moulting period in early-September, arriving in the winter quarters from late-September through October3. It remains gregarious throughout the winter3 (although it occurs in smaller, loose flocks than many other goose species)6 and roosts close to feeding areas3 in mixed-species flocks on lakes, rivers and flooded lands2. Habitat Breeding The species breeds near lakes, pools, rivers and streams in high Arctic tundra or the taiga forest zone1. Taiga nesting populations show a preference for scrubby birch Betula spp. forest3 and dense spruce forest with bogs or mires3, whereas tundra-based populations nest on damp tundra of moss, grass, sedge or scrub4 near river flood-plains (but above flood levels)2, 3, on Arctic islands and in Arctic coastal regions3. Non-breeding During the winter and on passage the species inhabits marshes, agricultural land1 (pastures, arable fields, rice-paddies)2, damp steppe grassland3, flood-lands, rivers and coastal shallows6 in open country1. It also roosts on lakes, rivers and flood-lands in Europe during this season2. Diet The species is herbivorous1, its diet consisting of herbs, grasses, sedges1 and mosses4, complemented during the breeding season by berries (e.g. from Empetrum or Vaccinium spp.)1. During the winter it feeds predominantly on agricultural land taking grain, beans, potatoes1 and sprouting winter cereal crops2. Breeding site The species builds a nest of vegetation in a shallow scrape on the ground1. Taiga breeders nest in bogs or mires within forested regions, placing nests within 400 m of open mire and within 2 km of open water, usually 50-100 cm above bog surfaces on hummocks that are safe from flooding2. Tundra breeders nest on dry hummocks and moss2. Management information An investigation carried out in one of the species' wintering areas (UK) found that it was most likely to forage on improved grassland or grasslands grazed by cattle that were a minimum of 5 ha in area, had an optimum sward height of c.20 cm and were at a distance of less than 9 km away from roosting sites10.

Systems
  • Terrestrial
  • Freshwater
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Depth range based on 52 specimens in 6 taxa.
Water temperature and chemistry ranges based on 21 samples.

Environmental ranges
  Depth range (m): 0 - 0
  Temperature range (°C): 1.712 - 11.768
  Nitrate (umol/L): 1.402 - 8.636
  Salinity (PPS): 31.635 - 35.334
  Oxygen (ml/l): 6.069 - 8.125
  Phosphate (umol/l): 0.273 - 0.574
  Silicate (umol/l): 0.987 - 3.347

Graphical representation

Temperature range (°C): 1.712 - 11.768

Nitrate (umol/L): 1.402 - 8.636

Salinity (PPS): 31.635 - 35.334

Oxygen (ml/l): 6.069 - 8.125

Phosphate (umol/l): 0.273 - 0.574

Silicate (umol/l): 0.987 - 3.347
 
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Molecular Biology and Genetics

Barcode

Locations of barcode samples

Collection Sites: world map showing specimen collection locations for Anser
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Statistics of barcoding coverage

Barcode of Life Data Systems (BOLD) Stats
                                                             
Specimen Records:43
Specimens with Sequences:33
Specimens with Barcodes:33
Public Records:19
Species:7
Species With Barcodes:7
  
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Barcode data

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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 very 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

Accidental visitor.

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IUCN

Least Concern.

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Threats

Threats

Major Threats
The species declined in the past due to hunting (resulting in mortality, injury and disturbance)1, 2, 8 and habitat loss1. Habitat degradation due to oil pollution7, 8, drainage, peat-extraction, changing management practices (decreased grazing and mowing in meadows leading to scrub over-growth) and forest clearance is a threat to breeding areas in Russia7, Norway and Sweden3. The species also suffers from human persecution3 and is susceptible to poisoning by pesticides used on agricultural land9.
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Wikipedia

Anser (bird)

See also Grey Goose (disambiguation)

The waterfowl genus Anser includes all grey geese and sometimes the white geese. It belongs to the true geese and swan subfamily (Anserinae). The genus has a Holarctic distribution, with at least one species breeding in any open, wet habitats in the subarctic and cool temperate regions of the Northern Hemisphere in summer. Some also breed further south, reaching into warm temperate regions. They mostly migrate south in winter, typically to regions in the temperate zone between the January 0 °C (32 °F) to 5 °C (41 °F) isotherms.

The genus contains ten living species, which span nearly the whole range of true goose shapes and sizes. The largest is the Greylag Goose at 2.5–4.1 kg (5.5–9.0 lb) weight, and the smallest is the Ross's Goose at 1.2–1.6 kg (2.6–3.5 lb). All have legs and feet that are pink, or orange, and bills that are pink, orange, or black. All have white under- and upper-tail coverts, and several have some extent of white on their heads. The neck, body and wings are grey or white, with black or blackish primary—and also often secondary—remiges (pinions). The closely related "black" geese in the genus Branta differ in having black legs, and generally darker body plumage.[1]

Contents

Systematics, taxonomy and evolution

Living species and taxonomy

The following white geese are commonly separated as the genus Chen, with one of them sometimes split off in the genus Philacte. They cannot be distinguished anatomically from Anser geese although there is some evidence of a distinct lineage in evaluations of molecular data.[citation needed] While some ornithological works traditionally include Chen within Anser,[2] the AOU and the IUCN are notable authorities that treat them as separate.[3]

Some authorities also treat some subspecies as distinct species (notably Tundra Bean Goose[4]) or as likely future species splits (notably Greenland White-fronted Goose).[5]

Fossil record

Numerous fossil species have been allocated to this genus. As the true geese are near-impossible to assign osteologically to genus, this must be viewed with caution. It can be assumed with limited certainty that European fossils from known inland sites belong into Anser. As species related to the Canada Goose have been described from the Late Miocene onwards in North America too, sometimes from the same localities as the presumed grey geese, it casts serious doubt on the correct generic assignment of the supposed North American fossil geese.[6] The Early Pliocene Branta howardae is one of the cases where doubts have been expressed about its generic assignment.[citation needed] Similarly, Heterochen = Anser pratensis seems to differ profoundly from other species of Anser and might be placed into a different genus; alternatively, it might have been a unique example of a grey goose adapted for perching in trees.[7]

The Maltese swan Cygnus equitum was occasionally placed into Anser, and Anser condoni is a synonym of Cygnus paloregonus.[8] A goose fossil from the Early-Middle Pleistocene of El Salvador is highly similar to Anser.[9] Given its age it is likely to belong to an extant genus, and biogeography indicates Branta as other likely candidate.

?Anser scaldii (Late Miocene of Antwerp, Belgium) may be a shelduck.

Relationship with humans and conservation status

Two species in the genus are of major commercial importance, having been domesticated as poultry: European domesticated geese are derived from the Greylag Goose, and Chinese and some African domesticated geese are derived from the Swan Goose.

Most species are hunted to a greater or lesser extent; in some areas, some populations are endangered by over-hunting. Most notably, the Lesser White-fronted Goose is listed by IUCN Red List as Vulnerable throughout its range, and due to overhunting and rampant habitat destruction, the population of the Swan Goose is on the verge of collapsing, leading to a listing as Endangered.[10]

Other species have benefited from reductions in hunting since the late 19th and early 20th centuries, with most species in western Europe and North America showing marked increases in response to protection[citation needed]. In some cases, this has led to conflicts with farming, when large flocks of geese graze crops in the winter.[citation needed]

Footnotes

  1. ^ Carboneras (1992)
  2. ^ E.g. Cramp (1977), Madge & Burn (1988), Handbook of Birds of the World (Carboneras 1992), and the 2006 British Ornithologists' Union checklist (Dudley et al. 2006)
  3. ^ AOU (1998), IUCN (2007)
  4. ^ Banks et al. (2007), van den Berg (2007)
  5. ^ Fox & Stroud (2002)
  6. ^ Brodkorb (1964), Short (1970), Livezey (1986)
  7. ^ Short (1970) considers this bird to be somewhat reminiscent of geese and swans, shelducks, and the "Cairinini" or "perching ducks". The latter are now known to be a paraphyletic assemblage of miscellaneous waterfowl the morphological similarities of which is the product of convergent evolution towards being able to perch in trees (Livezey 1986).
  8. ^ Brodkorb (1964)
  9. ^ A left humerus (specimen MUHNES 2SSAP30-853) and a left clavicle (specimen MUHNES 2SSAP30-545), apparently of a single bird: Cisneros (2005).
  10. ^ IUCN (2007)

References

  • American Ornithologists' Union (AOU) (1998): Check-list of North American Birds: the species of birds of North America from the Arctic through Panama, including the West Indies and Hawaiian Islands (7th ed., 41st supplement). American Ornithologists' Union and Allen Press, Washington, D.C. and Lawrence, Kansas, USA. ISBN 1-891276-00-X PDF fulltext
  • Banks, Richard C.; Chesser, R. Terry; Cicero, Carla; Dunn, Jon L.; Kratter, Andrew W.; Lovette, Irby J.; Rasmussen, Pamela C.; Remsen, J.V. Jr; Rising, James D. & Stotz, Douglas F. (2007): Forty-eighth Supplement to the American Ornithologists' Union Check-List of North American Birds. Auk 124(3): 1109-1115. DOI:10.1642/0004-8038(2007)124[1109:FSTTAO]2.0.CO;2 PDF fulltext
  • Brodkorb, Pierce (1964): Catalogue of Fossil Birds: Part 2 (Anseriformes through Galliformes). Bulletin of the Florida State Museum 8(3): 195-335. PDF or JPEG fulltext
  • Carboneras, Carles (1992): Family Anatidae (Ducks, Geese and Swans). In: del Hoyo, Josep; Elliott, Andrew & Sargatal, Jordi (eds.): Handbook of Birds of the World (Volume 1: Ostrich to Ducks): 536-629, plates 40-50. Lynx Edicions, Barcelona. ISBN 84-87334-10-5
  • Cisneros, Juan Carlos (2005): New Pleistocene vertebrate fauna from El Salvador. [English with Portuguese abstract] Revista Brasileira de Paleontologia 8(3): 239-255. PDF fulltext
  • Cramp, S. (1977): The Birds of the Western Palearctic. Oxford. ISBN 0-19-857358-8
  • Dudley, Steve P.; Gee, Mike; Kehoe, Chris; Melling, Tim M. & The British Ornithologists' Union Records Committee (BOURC) (2006): The British List: A Checklist of Birds of Britain (7th edition). Ibis 148(3): 526–563. doi:10.1111/j.1474-919X.2006.00603.x PDF fulltext
  • Fox, A.D. & Stroud, D.A. (2002): Greenland White-fronted Goose. Birds of the Western Palearctic Update 4(2): 65-88.
  • IUCN (2007): 2007 IUCN Red List of Threatened Species.
  • Livezey, Bradley C. (1986): A phylogenetic analysis of recent anseriform genera using morphological characters. Auk 103(4): 737-754. PDF fulltext
  • Madge, Steve & Burn, Hilary (1987): Wildfowl : an identification guide to the ducks, geese and swans of the world. Christopher Helm, London. ISBN 0-7470-2201-1
  • Short, Lester L. (1970): A new anseriform genus and species from the Nebraska Pliocene. Auk 87(3): 537-543. DjVu fulltext PDF fulltext
  • van den Berg, Arnoud B. (2007): Lijst van Nederlandse vogelsoorten ["List of Dutch bird taxa²]. [Dutch and English] PDF fulltext
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Bean Goose

The Bean Goose is a goose that breeds in northern Europe and Asia. It has two distinct varieties, one inhabiting taiga habitats and one inhabiting tundra. These are recognised as separate species by the American Ornithologists' Union, but are considered a single species by other authorities, such as the British Ornithologists' Union. It is migratory and winters further south in Europe and Asia.

Contents

Description

The length ranges from 68 to 90 centimetres (27–35 in), wingspan from 140 to 174 centimetres (55–69 in) and weight from 1.7–4 kilograms (3.7–8.8 lb).[2] In the nominate subspecies, males average 3.2 kg (7.1 lb) and females average 2.84 kg (6.3 lb).[2] The bill is black at the base and tip, with an orange band across the middle; the legs and feet are also bright orange.

The upper wing-coverts are dark brown, as in the White-fronted Goose (Anser albifrons) and the Lesser White-fronted Goose (A. erythropus), but differing from these in having narrow white fringes to the feathers.

The voice is a loud honking, higher pitched in the smaller subspecies.

The closely related Pink-footed Goose (A. brachyrhynchus) has the bill short, bright pink in the middle, and the feet also pink, the upper wing-coverts being nearly of the same bluish-grey as in the Greylag Goose. In size and bill structure, it is very similar to Anser fabalis rossicus, and in the past was often treated as a sixth subspecies of Bean Goose.

Taxonomy

The English and scientific names of the Bean Goose come from its habit in the past of grazing in bean field stubbles in winter (Latin faba, a bean).

Taiga Bean Goose (Anser fabalis sensu stricto) on background, Tundra Bean Goose (Anser serrirostris) on foreground and Greylag Goose (Anser anser) on the right, at Spaarndam, Noord-Holland, the Netherlands
A flock of Tundra Bean Geese

There are five subspecies, with complex variation in body size and bill size and pattern; generally, size increases from north to south and from west to east. Some ornithologists (including AOU 2007) split them into two species based on breeding habitat, whether in forest bogs in the subarctic taiga, or on the arctic tundra.

Taiga Bean Goose (Anser fabalis sensu stricto) (Latham, 1787)
  • A. f. fabalis (Latham, 1787). Scandinavia east to the Urals. Large; bill long and narrow, with broad orange band. Anser fabalis fabalis is one of the species to which the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) applies.
  • A. f. johanseni (Delacour, 1951). West Siberian taiga. Large; bill long and narrow, with narrow orange band.
  • A. f. middendorffii (Severtzov, 1873). East Siberian taiga. Very large; bill long and stout, with narrow orange band.
Tundra Bean Goose (Anser serrirostris, if treated as a distinct species) (Swinhoe, 1871)
  • A. s. rossicus (Buturlin, 1933). Northern Russian tundra east to the Taimyr Peninsula. Small; bill short and stubby, with narrow orange band. Anser fabalis rossicus is one of the species to which the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) applies.
  • A. s. serrirostris (Swinhoe, 1871). East Siberian tundra. Large; bill long and stout, with narrow orange band.

Distribution

The Bean Goose is a rare winter visitor to Britain. There are two regular wintering flocks of Taiga Bean Goose, in the Yare Valley, Norfolk and the Avon Valley, Scotland. A formerly regular flock in Dumfries and Galloway no longer occurs there. The Tundra Bean Goose has no regular wintering sites, but is found in small groups among other grey goose species – among the most regular localities are WWT Slimbridge, Gloucestershire and Holkham Marshes, Norfolk.

References

  1. ^ BirdLife International (2004). Anser fabalis. 2006. IUCN Red List of Threatened Species. IUCN 2006. www.iucnredlist.org. Retrieved on 11 May 2006.
  2. ^ a b CRC Handbook of Avian Body Masses by John B. Dunning Jr. (Editor). CRC Press (1992), ISBN 978-0-8493-4258-5.

Further reading

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