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Its dark grey, rather than brown plumage, and the dark bands on the grey tail distinguish it from the other pigeon endemic to the Canary Islands, the [[Laurel Pigeon]].
Its dark grey, rather than brown plumage, and the dark bands on the grey tail distinguish it from the other pigeon endemic to the Canary Islands, the [[Laurel Pigeon]].


Mainly dark grey with blacker flight feathers and paler grey tail with dark terminal band, hindneck with green and pink gloss and reddish tinge to breast. Red bill and yellow eye. Similar: Only likely to be confused with White-tailed Laurel Pigeon C. junoniae or dark Feral Pigeon.Voice: Guttural mournful cooing. Hints: Look for birds flying low and fast over laurel forest.
Mainly dark grey with blacker flight feathers and paler grey tail with dark terminal band, hindneck with green and pink gloss and reddish tinge to breast. Red bill and yellow eye. Similar: Only likely to be confused with White-tailed Laurel Pigeon Columba junoniae or dark Feral Pigeon. The voice is a guttural mournful cooing. Hints: Look for birds flying low and fast over laurel forest.
Its flight is quick, performed by regular beats, with an occasional sharp flick of the wings, characteristic of pigeons in general. It takes off with a loud clattering.
Its flight is quick, performed by regular beats, with an occasional sharp flick of the wings, characteristic of pigeons in general. It takes off with a loud clattering.


The call is a hoarse cooing.
The call is a hoarse cooing.
== Ecollogy==

Breeding occurs in in trees especially in February-June.
==Distribution and population==
==Distribution and population==


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In 2007, the species was estimated by SEO Sociedad Española de Ornitología, BirdLife in Spain to number 5,000-20,000 individuals.
In 2007, the species was estimated by SEO Sociedad Española de Ornitología, BirdLife in Spain to number 5,000-20,000 individuals.


It occurs in dense laurel forest in mountainous areas, especially in ravines; also in heath of Myrica faya and Erica arborea, and sometimes in rather open areas, e.g. cultivation. It spends the hottest part of the day in deep shade. It feeds mainly on fruit but also takes grain and occasionally buds, leaves and shoots. It will gather in large concentrations on fruiting trees, plucking berries from the tree but also feeding on the ground. Breeding occurs in January-September. It makes some altitudinal movements to take advantage of ripe cereals and fruit at lower elevations in late summer.
It occurs in dense [[laurel forest]] in mountainous areas, especially in ravines; also in heath of Myrica faya and Erica arborea, and sometimes in rather open areas, e.g. cultivation. It spends the hottest part of the day in deep shade. It feeds mainly on fruit but also takes grain and occasionally buds, leaves and shoots. It will gather in large concentrations on fruiting trees, plucking berries from the tree but also feeding on the ground. It makes some altitudinal movements to take advantage of ripe cereals and fruit at lower elevations in late summer.


Threats Historical declines resulted from intensive exploitation of laurel forests. The extent of forest loss has slowed, although fragmentation has continued in some areas as forests are exploited for poles and tool handles. A small amount of illegal hunting occurs at drinking sites. As it is a tree-nesting species, predation by introduced mammals including rats is of less significance than for C. junoniae but it remains a potential threat, the impact of which has not been fully assessed1. Grazing pressure from sheep is leading to habitat degradation on La Gomera and at El Hierro. Forest fires also pose a moderate threat to its habitat. Recreational activities cause some disturbance in the breeding season. The species is potentially threatened by outbreaks of Newcastle Disease and Tuberculosis.
Threats Historical declines resulted from intensive exploitation of laurel forests. The extent of forest loss has slowed, although fragmentation has continued in some areas as forests are exploited for poles and tool handles. A small amount of illegal hunting occurs at drinking sites. As it is a tree-nesting species, predation by introduced mammals including rats is of less significance than for C. junoniae but it remains a potential threat, the impact of which has not been fully assessed1. Grazing pressure from sheep is leading to habitat degradation on La Gomera and at El Hierro. Forest fires also pose a moderate threat to its habitat. Recreational activities cause some disturbance in the breeding season. The species is potentially threatened by outbreaks of Newcastle Disease and Tuberculosis.


The natural habitat is tall [[laurisilva]] forest or dense [[Erica arborea|tree heath]]s which are cloud-covered for much of the year.<ref name=BWP> Snow (1998) p. 848. </ref> The forests consist mainly of [[Laurus azorica|Azores Laurel]], ''[[Oreodaphne foetens]]'',<ref>{{cite book|author=Hartert, E|title= Die Vögel der paläarktischen Fauna. Volume 2|publisher=H. Friedlander & Sohn| location = Berlin|year=1912–21|page=1480|language = German|url=http://www.archive.org/stream/dievgelderpal02hart#page/1480/mode/1up}}</ref> [[Ocotea foetens|Til]], [[Persea indica|Madeira Mahogany]], [[Appolonias barbujana|Canary Laurel]], [[Myrica faya|Faya]], [[Clethra arborea|Lily of the Valley Tree]] and the [[Picconia excelsa|Picconia]]. The Trocaz Pigeon prefers [[Old-growth forest|primary forest]]s, but [[secondary growth]] is used for feeding, and agricultural land is also visited, especially at times of fruit shortage.<ref name= Gibbs188/> Most of the pigeons are found below 1000&nbsp;m (3300&nbsp;ft), and their prime environment appears to be steep ravine-indented slopes along artificial watercourses, with the occasional large dead laurel tree and much tree heath.<ref name=BWP/> This species is highly mobile between different areas at different times of year.

It was very abundant when the islands were first colonised by humans, but was extirpated. The losses on the islands were largely due to deforestation for wood and to create agricultural and grazing land.

The exclusion of livestock from the native forest allows it to regenerate and create more suitable habitat. Some illegal hunting and poisoning continues because of the damage this pigeon can do to crops. Perhaps the main limiting factor on the rate at which the pigeon increases its numbers is eggs and young being taken by introduced [[Black rat|Black Rats]]. It is now classed as [[Near Threatened]] on the [[IUCN Red List]], an improvement on its [[Threatened species|Threatened]] status in 1988. This species is protected under the [[European Union]] [[Birds Directive]], and the laurel forests under the [[Habitats Directive]].
==Taxonomy==
The genus ''[[Columba (genus)|Columba]]'' is the largest within the [[Columbidae|pigeon family]], and has the widest distribution. Its members are typically pale grey or brown, often with white head or neck markings or iridescent green or purple patches on the neck and breast. The neck feathers may be stiffened and aligned to form grooves. One of several subgroups within ''Columba'' consists of the widespread Eurasian Common Wood Pigeon, Bolle's Pigeon, the Trocaz Pigeon, and the African [[Afep Pigeon]]. The two [[Macaronesia]]n endemic pigeons, Bolle's and Trocaz, are thought to be derived from isolated island populations of ''C.&nbsp;palumbus''.<ref name= Gibbs175>Gibbs (2000) p. 175.</ref>

The Atlantic archipelagos of the [[Canaries]], [[Azores]], and [[Madeira]] have a volcanic origin and they have never been part of a continent. The formation of Madeira started in the [[Miocene]] and the island was substantially complete by 700,000 years ago.<ref name = gvp>{{cite web| author = | title= Madeira | work=Global Volcanism Program | url= http://www.volcano.si.edu/world/volcano.cfm?vnum=1802-12- | publisher=Smithsonian Institution }} Retrieved 20 July 2010</ref> At various times in the past, the major islands of these archipelagos were all colonised by ancestral wood pigeons, which evolved on their respective islands in isolation from the mainland populations. [[mitochondrion|Mitochondrial]] and [[cell nucleus|nuclear]] [[DNA]] sequences suggest that the ancestor of Bolle's Pigeon may have arrived in the Canaries about 5&nbsp;[[mya (unit)|mya]], but an older lineage that gave rise to another Canarian endemic, the [[Laurel Pigeon]], ''C.&nbsp;junoniae'', may date from 20&nbsp;mya.<ref name= Gonzalez>{{cite journal | last= Gonzalez | first= Javier | coauthors= Castro, Guillermo Delgado; Garcia-del-Rey, Eduardo; Berger, Carola; Wink, Michael | year= 2009| title= Use of mitochondrial and nuclear genes to infer the origin of two endemic pigeons from the Canary Islands | journal= Journal of Ornithology | volume= 150 | issue = 2 | pages= 357–367 | url = |format = | doi = 10.1007/s10336-008-0360-4 }}</ref> The most recent wood pigeon arrival on Macaronesia was that which gave rise to the subspecies ''C.&nbsp;palumbus maderensis''.

The [[Trocaz Pigeon]] was formally described in 1829 by [[Karl Heineken]]. He recognised it as different from the now-extinct local form of the [[Madeiran Wood Pigeon]] a sub-species of the [[Common Wood Pigeon]]. This is a [[Monotypic taxon|monotypic]] species, although in the past the canarian Bolle's Pigeon was sometimes regarded as a [[subspecies]] of the Trocaz Pigeon.<ref name= martin>{{cite journal | last= Martin | first= A | year= 1985| title= Première observation du pigeon Trocaz (''Columba trocaz bollii'') à l'Ile de Hierro (Iles Canaries) | journal= Alauda | language = French | volume= 53 | issue = 2 | pages= 137–140}}</ref>


==References==
==References==

Revision as of 22:13, 29 September 2011

Bolle's Pigeon
Scientific classification
Kingdom:
Phylum:
Class:
Order:
Family:
Genus:
Species:
C. bollii
Binomial name
Columba bollii
Godman, 1872

The Bolle's Pigeon (Columba bollii) is a member of the family Columbidae, doves and pigeons, which is endemic to the Canary Islands, Spain. This bird is named after the German naturalist Carl Bolle, who was the first to distinguish it from the Laurel Pigeon.

Description

36 cm. Large dark grey pigeon. At 37–40 cm, it looks like a very dark Wood Pigeon. It is a basically dark grey bird, with a pinkish breast. It lacks any white markings, which together with its darker plumage distinguishes it from the other species.

Its dark grey, rather than brown plumage, and the dark bands on the grey tail distinguish it from the other pigeon endemic to the Canary Islands, the Laurel Pigeon.

Mainly dark grey with blacker flight feathers and paler grey tail with dark terminal band, hindneck with green and pink gloss and reddish tinge to breast. Red bill and yellow eye. Similar: Only likely to be confused with White-tailed Laurel Pigeon Columba junoniae or dark Feral Pigeon. The voice is a guttural mournful cooing. Hints: Look for birds flying low and fast over laurel forest. Its flight is quick, performed by regular beats, with an occasional sharp flick of the wings, characteristic of pigeons in general. It takes off with a loud clattering.

The call is a hoarse cooing.

Ecollogy

Breeding occurs in in trees especially in February-June.

Distribution and population

It is a resident breeder in the mountain laurisilva forest zone. Bolle's Pigeon builds a stick nest in a tree, laying one white egg. Columba bollii occurs on Tenerife particularly at Anaga and Teno, La Palma in a restricted area of the north-east), La Gomera in Garajonay National Park with some birds outside the park, and El Hierro (where it occurs in Golfo and Sabinosa in the Canary Islands, Spain. It may formerly have occurred on Gran Canaria, as bones similar to those of a laurel pigeon have been found and there is a possible sight record from the late 19th century. It was common in the past, but disappeared from many areas owing to clearance of laurel forest in the islands. More recently the rate of laurel forest clearance has been slowed or stopped. Population estimates for the species are 1,160-1,315 birds in 1980, 6,000 individuals in 2001, and 5,000-20,000 most recently. Whether these figures reveal genuine population increases is unclear, but the area of occupied territory appears to be expanding and despite several potential threats the population is at least stable, probably increasing.

In 2007, the species was estimated by SEO Sociedad Española de Ornitología, BirdLife in Spain to number 5,000-20,000 individuals.

It occurs in dense laurel forest in mountainous areas, especially in ravines; also in heath of Myrica faya and Erica arborea, and sometimes in rather open areas, e.g. cultivation. It spends the hottest part of the day in deep shade. It feeds mainly on fruit but also takes grain and occasionally buds, leaves and shoots. It will gather in large concentrations on fruiting trees, plucking berries from the tree but also feeding on the ground. It makes some altitudinal movements to take advantage of ripe cereals and fruit at lower elevations in late summer.

Threats Historical declines resulted from intensive exploitation of laurel forests. The extent of forest loss has slowed, although fragmentation has continued in some areas as forests are exploited for poles and tool handles. A small amount of illegal hunting occurs at drinking sites. As it is a tree-nesting species, predation by introduced mammals including rats is of less significance than for C. junoniae but it remains a potential threat, the impact of which has not been fully assessed1. Grazing pressure from sheep is leading to habitat degradation on La Gomera and at El Hierro. Forest fires also pose a moderate threat to its habitat. Recreational activities cause some disturbance in the breeding season. The species is potentially threatened by outbreaks of Newcastle Disease and Tuberculosis.

The natural habitat is tall laurisilva forest or dense tree heaths which are cloud-covered for much of the year.[2] The forests consist mainly of Azores Laurel, Oreodaphne foetens,[3] Til, Madeira Mahogany, Canary Laurel, Faya, Lily of the Valley Tree and the Picconia. The Trocaz Pigeon prefers primary forests, but secondary growth is used for feeding, and agricultural land is also visited, especially at times of fruit shortage.[4] Most of the pigeons are found below 1000 m (3300 ft), and their prime environment appears to be steep ravine-indented slopes along artificial watercourses, with the occasional large dead laurel tree and much tree heath.[2] This species is highly mobile between different areas at different times of year.

It was very abundant when the islands were first colonised by humans, but was extirpated. The losses on the islands were largely due to deforestation for wood and to create agricultural and grazing land.

The exclusion of livestock from the native forest allows it to regenerate and create more suitable habitat. Some illegal hunting and poisoning continues because of the damage this pigeon can do to crops. Perhaps the main limiting factor on the rate at which the pigeon increases its numbers is eggs and young being taken by introduced Black Rats. It is now classed as Near Threatened on the IUCN Red List, an improvement on its Threatened status in 1988. This species is protected under the European Union Birds Directive, and the laurel forests under the Habitats Directive.

Taxonomy

The genus Columba is the largest within the pigeon family, and has the widest distribution. Its members are typically pale grey or brown, often with white head or neck markings or iridescent green or purple patches on the neck and breast. The neck feathers may be stiffened and aligned to form grooves. One of several subgroups within Columba consists of the widespread Eurasian Common Wood Pigeon, Bolle's Pigeon, the Trocaz Pigeon, and the African Afep Pigeon. The two Macaronesian endemic pigeons, Bolle's and Trocaz, are thought to be derived from isolated island populations of C. palumbus.[5]

The Atlantic archipelagos of the Canaries, Azores, and Madeira have a volcanic origin and they have never been part of a continent. The formation of Madeira started in the Miocene and the island was substantially complete by 700,000 years ago.[6] At various times in the past, the major islands of these archipelagos were all colonised by ancestral wood pigeons, which evolved on their respective islands in isolation from the mainland populations. Mitochondrial and nuclear DNA sequences suggest that the ancestor of Bolle's Pigeon may have arrived in the Canaries about 5 mya, but an older lineage that gave rise to another Canarian endemic, the Laurel Pigeon, C. junoniae, may date from 20 mya.[7] The most recent wood pigeon arrival on Macaronesia was that which gave rise to the subspecies C. palumbus maderensis.

The Trocaz Pigeon was formally described in 1829 by Karl Heineken. He recognised it as different from the now-extinct local form of the Madeiran Wood Pigeon a sub-species of the Common Wood Pigeon. This is a monotypic species, although in the past the canarian Bolle's Pigeon was sometimes regarded as a subspecies of the Trocaz Pigeon.[8]

References

  1. ^ Template:IUCN2006 Database entry includes a brief justification of why this species is near threatened
  2. ^ a b Snow (1998) p. 848.
  3. ^ Hartert, E (1912–21). Die Vögel der paläarktischen Fauna. Volume 2 (in German). Berlin: H. Friedlander & Sohn. p. 1480.
  4. ^ Cite error: The named reference Gibbs188 was invoked but never defined (see the help page).
  5. ^ Gibbs (2000) p. 175.
  6. ^ "Madeira". Global Volcanism Program. Smithsonian Institution. Retrieved 20 July 2010
  7. ^ Gonzalez, Javier (2009). "Use of mitochondrial and nuclear genes to infer the origin of two endemic pigeons from the Canary Islands". Journal of Ornithology. 150 (2): 357–367. doi:10.1007/s10336-008-0360-4. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  8. ^ Martin, A (1985). "Première observation du pigeon Trocaz (Columba trocaz bollii) à l'Ile de Hierro (Iles Canaries)". Alauda (in French). 53 (2): 137–140.