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Overview
Distribution
Range
- Clements, J. F., T. S. Schulenberg, M. J. Iliff, B.L. Sullivan, C. L. Wood, and D. Roberson. 2012. The eBird/Clements checklist of birds of the world: Version 6.7. Downloaded from http://www.birds.cornell.edu/clementschecklist/downloadable-clements-checklist
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UNESCO-IOC Register of Marine Organisms
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1318
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Brown, L.H., E.K. Urban & K. Newman (1982). The Birds of Africa, Volume I. Academic Press, London.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6168
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Gordon, D. (Ed.) (2009). New Zealand Inventory of Biodiversity. Volume One: Kingdom Animalia. 584 pp
http://www.marinespecies.org/porifera/porifera.php?p=sourcedetails&id=145244
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Range Description
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National Distribution
United States
Origin: Native
Regularity: Regularly occurring
Currently: Present
Confidence: Confident
Type of Residency: Breeding
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Global Range: (>2,500,000 square km (greater than 1,000,000 square miles)) BREEDS: Revillagigedo Islands (western Mexico), Hawaii (Kure east to Kauai and Oahu, and on small islets around main islands), central and western Pacific islands south to southern Australia and New Zealand, and Indian Ocean. RANGES at sea in Pacific off west coast of Middle America and South America (from Baja California, the Tres Marias Islands, and Nayarit south to Panama, Colombia, and Ecuador, and throughout most of central and western Pacific Ocean north to Japan and Formosa; and in Indian Ocean (AOU 1983).
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Physical Description
Size
Type Information
Catalog Number: USNM 113445
Collection: Smithsonian Institution, National Museum of Natural History, Department of Vertebrate Zoology, Division of Birds
Sex/Stage: unknown;
Preparation: Skin: Whole
Collector(s): V. Knudsen
Locality: Kauai County, Kauai Island, Main Hawaiian Islands, North Pacific Ocean
- Type: Stejneger. November 8, 1888. Proc. U.S. Nat. Mus. 11: 93.
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Ecology
Habitat
Habitat and Ecology
Systems
- Terrestrial
- Marine
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Water temperature and chemistry ranges based on 100 samples.
Environmental ranges
Depth range (m): 0 - 0
Temperature range (°C): 10.401 - 28.903
Nitrate (umol/L): 0.037 - 3.951
Salinity (PPS): 33.176 - 36.318
Oxygen (ml/l): 4.556 - 6.574
Phosphate (umol/l): 0.145 - 0.674
Silicate (umol/l): 1.374 - 6.162
Graphical representation
Temperature range (°C): 10.401 - 28.903
Nitrate (umol/L): 0.037 - 3.951
Salinity (PPS): 33.176 - 36.318
Oxygen (ml/l): 4.556 - 6.574
Phosphate (umol/l): 0.145 - 0.674
Silicate (umol/l): 1.374 - 6.162
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Comments: Pelagic. Nests in burrow, crevice, sometimes on ground surface (usually in shade); on offshore islet, atoll, barren headland. Typical breeding area is low, flat islands and sand spits with little or no vegetation. Integrity of the burrow demands either firm soil or some vegetation to hold soil together (Whittow 1997). Uses slopes of extinct volcanoes and old volcanic craters in main Hawaiian Islands. Usually no tall woody plants in nesting areas; these would impair flight paths of birds to and from nesting burrows, but grass can be quite long and dense in vicinity of burrow. Readily uses artificial burrows (Byrd 1979, Byrd et al. 1983). Generally returns to same nesting area in successive years.
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Migration
Non-Migrant: No. All populations of this species make significant seasonal migrations.
Locally Migrant: No. No populations of this species make local extended movements (generally less than 200 km) at particular times of the year (e.g., to breeding or wintering grounds, to hibernation sites).
Locally Migrant: Yes. At least some populations of this species make annual migrations of over 200 km.
In Hawaii, migrants begin to arrive in nesting areas in March; depart in November (Byrd et al. 1983). Mostly January-March off coast of Costa Rica (Stiles and Skutch 1989).
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Trophic Strategy
Population Biology
General Ecology
Seasonally in large flocks well off coast (Costa Rica, Stiles and Skutch 1989). Nesting success on larger islands in Hawaii often reduced by introduced predators (mongoose, dogs, cats, common myna) (Byrd et al. 1983).
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Life History and Behavior
Cyclicity
Comments: Flight activity at nesting areas primarily nocturnal or crepuscular.
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Life Expectancy
Lifespan, longevity, and ageing
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Reproduction
In Hawaii, eggs are laid in June. Clutch size is 1. Incubation, by both sexes, lasts 51-55 days. Hawaii: nestling period lasts 99-115 days; fledging peaks in mid-November (Byrd et al. 1983). Multiannual pair bond.
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Puffinus pacificus
There are 8 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.
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Download FASTA File
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Statistics of barcoding coverage: Puffinus pacificus
Public Records: 8
Specimens with Barcodes: 17
Species With Barcodes: 1
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Conservation
Conservation Status
IUCN Red List Assessment
Red List Category
Red List Criteria
Version
Year Assessed
Assessor/s
Reviewer/s
Contributor/s
Justification
History
- 2008Least Concern
- 2004Least Concern
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National NatureServe Conservation Status
United States
Rounded National Status Rank: NNRB - Unranked
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Trends
Population
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Threats
Comments: Fledglings are attracted to lights on Oahu in fall; many hit by cars or killed by cats or dogs (Shallenberger 1984).
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Wikipedia
Wedge-tailed Shearwater
The Wedge-tailed Shearwater, Puffinus pacificus is a medium-large shearwater in the seabird family Procellariidae. It is one of the shearwater species that is sometimes referred to as a Muttonbird, like the Sooty Shearwater of New Zealand and the Short-tailed Shearwater of Australia. It ranges across from throughout the tropical Pacific and Indian Ocean roughly between latitudes 35°N and 35°S. It breeds in islands such as off Japan, the Islas Revillagigedo, the Hawaiian Islands, the Seychelles and off Western Australia.
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Description
The Wedge-tailed Shearwater is the largest of the tropical shearwaters. There are two colour morphs of the species, dark and pale; the pale morphs predominate in the North Pacific, the dark morph elsewhere. However, both morphs exist in all populations, and bear no relation to sex or breeding condition. The pale morph has grey-brown plumage on the back, head and upperwing, and whiter plumage below. The darker morph has the same dark grey-brown plumage over the whole body. The species’ common name is derived from the large wedge-shaped tail, which may help the species glide. The bill is dark and legs are flesh coloured, with the legs set far back on the body (in common with the other shearwaters) as an adaptation for swimming.
This species is related to the pan-Pacific Buller's Shearwater, which differs much in color pattern, but also has a wedgetail and a thin black bill (Austin, 1996; Austin et al., 2004). They make up the Thyellodroma group, a superspecies in the large shearwaters of the proposed genus Ardenna (Penhallurick & Wink, 2004).
Diet
Wedge-tailed Shearwaters feed pelagically on fish, squid and crustaceans. 66% of their diet is fish, of which the most commonly taken is goatfish. It was thought that the species mostly took food from surface feeding, observations of feeding Wedge-tails suggested that contact-dipping, where birds flying close to the surface snatch prey from the water was the most commonly used hunting technique. However, a 2001 study which deployed maximum depth recorders found that 83% of Wedge-tails dived during foraging trips with a mean maximum depth of 14 m and that they could achieve a depth of 66 m (Burger, 2001).
Breeding behaviour
The Wedge-tailed Shearwater breeds in colonies on small tropical islands. Breeding seasons vary depending on location, with synchronised breeding seasons more common at higher latitudes. Northern hemisphere birds begin breeding around February, southern hemisphere birds begin around September. Wedge-tailed Shearwaters display natal philopatry, returning to their natal colony to begin breeding at the age of four.
Wedge-tailed Shearwaters are monogamous, forming a long term pair bond that lasts for several years. Divorce between pairs occurs after breeding seasons that end in failure. Nesting either in burrows or sometimes on the surface under cover. Pairs call frequently as a pair, both to reinforce the pair bond and warn intruders away from their territory. Parents also call to their chicks. The call is long, with an inhaling component (OOO) and exhaling component (err); their Hawaiian name ua’u kani means moaning petrel. Both sexes participate in digging a burrow, or repairing the burrow from last year. Nesting burrows of other species are also used. The breeding season of the Bonin Petrel in Hawaii is timed to avoid that of the Wedge-tail; in years where Bonin Petrel chicks are still in burrows when Wedge-tails return to begin breeding these chicks are killed or evicted. It attends these colonies nocturnally, although non-breeding Wedge-tails are often seen at the surface throughout the day and breeding birds will rest outside their burrows before laying.
Both sexes undertake a prelaying exodus in order to build up energy reserves, this usually lasts around 28 days. A single egg is laid, if that egg is lost then the pair will not attempt another that season. After laying the male usually undertakes the first incubation stint. Both sexes incubate the egg, in stints that can last up to 13 days. Incubation takes around 50 days. After hatching the chick is brooded for up to six days, until it is able to thermoregulate, after which it is left alone in the nest while both parents hunt for food. It is initially fed with stomach oil, an energy rich waxy oil of digested prey created in the parent’s gut; later it is fed both solids and stomach oil. Like many procellariids Wedge-tailed Shearwater parents alternate long and short trips to provide food, with the parents alternating between short foraging trips (1-4 days) and long trips (about 8 days), the two parents coordinating their feeding effort. Chicks increase in size to 560 g (larger than the adults) then drop to around 430 g before fledging. Fledging occurs after 103-115 days, after which the chick is independent of the adult.
Known breeding colonies include:
- Heron Island, Australia
- Lady Elliot Island, Australia
- Lord Howe Island, Australia
- Montague Island, Southern New South Wales, Australia
- North West Island, Australia
- Muttonbird Island, Coffs Harbour, Northern New South Wales, Australia
- Manana Island, Hawaii, USA
- Ilot Maitre, Noumea, New Caledonia
Media
References
- Austin, Jeremy J. (1996): Molecular Phylogenetics of Puffinus Shearwaters: Preliminary Evidence from Mitochondrial Cytochrome b Gene Sequences. Molecular Phylogenetics and Evolution 6(1): 77–88. doi:10.1006/mpev.1996.0060 (HTML abstract)
- Austin, Jeremy J.; Bretagnolle, Vincent & Pasquet, Eric (2004): A global molecular phylogeny of the small Puffinus shearwaters and implications for systematics of the Little-Audubon's Shearwater complex. Auk 121(3): 847–864. DOI: 10.1642/0004-8038(2004)121[0847:AGMPOT]2.0.CO;2 HTML abstract
- BirdLife International (2004). Puffinus pacificus. 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
- Burger, A. (2001): Diving depths of Shearwaters Auk 118(3):755–759 DOI: 10.1642/0004-8038(2001)118[0755:DDOS]2.0.CO;2 HTML abstract HTML fulltext (without images)
- Congdon, Brad C.; Krockenberger, Andrew K., & Smithers, Brian V. (2005): Dual-foraging and co-ordinated provisioning in a tropical Procellariiform, the wedge-tailed shearwater. Marine Ecology Progress Series (310): 293-301.
- Penhallurick, John & Wink, Michael (2004): Analysis of the taxonomy and nomenclature of the Procellariformes based on complete nucleotide sequences of the mitochondrial cytochrome b gene. Emu 104(2): 125-147. doi:10.1071/MU01060 (HTML abstract)
Unreviewed



