MEASO Biota Assessment pages should be titled: MEASO Biota: Species name/group

The purpose of these assessment pages is to summarise basic information for a species or taxonomic group and how the status and ecology of the group may be changing over time (link here to the framework for assessing biota within the MEASO framework):

  • General Description
  • Autecology (species' ecology: life history, phenology, food, energetics, movement, rate processes)
  • Habitat (physical environment, biological dependencies,Relationships, thresholds and limits )
  • Population (distribution, status and trends in abundance)
  • Synecology (species interactions: food webs, competitors)
  • Assessments of status (critical state of population e.g. IUCN Red List)
  • Contributing authors and experts
  • References

Authors are encouraged to use the spatial partitioning of the marine ecosystem assessment (sectors etc - link here), as well as circumpolar information where available. Assessments of change can include, where possible, historical change, current trends and prognoses for future change. Generalities should be avoided and, instead, replaced with specific quantities of change and parameters, including error/uncertainty.  Qualitative statements are acceptable provided the reasons for the qualitative conclusions are given, along with the scope for the application of the statements, and the uncertainty surrounding them. 

In the case of Parameter Tables, authors are asked to include estimates of parameters and their error, wherever possible. Delete parameters that are not relevant.  Add parameters that are relevant but not included in the tables.  The reference/s estimating the parameters should be cited, along with any statements as to the maturity of the estimates if known (e.g. under development, personal communications, future work is examining.....).  For some species, life history information and parameters are co-opted from areas outside of the subject area, e.g. from outside the Southern Ocean.  This proxy information is reasonable to include.  Please include also the rationale for co-opting these data, and citations.

Biota pages need to be written concisely, well-referenced, and using the uncertainty language of the IPCC. In the first instance, references can be from peer-reviewed literature, reports that are publicly available or references in the grey literature that could be obtained from repositories. If the information is known but the references cannot be sourced in the first instance that put a placeholder for filling in the citation.  This is useful for translating common ideas into this assessment without worrying about the pedigree of the idea in the first instance.

Under each heading is a list of information (in red italics) that is desirable for that section. Please do not change these main headings. If needed, a section can be further subdivided. Please delete the red italics and the instructions window from the page when it is completed (when the page is in edit mode you can select it for deletion).

On photographs, figures and tables:

If these are taken from publications or libraries that require recognition of copyright then we need to secure the necessary permissions to include them on these pages.  Put a placeholder with a reference to the material and then seek permission for use.  Or contact us and we will undertake this process.

All materials taken from libraries or references need to be cited appropriately, including photographs and text from web sites.  See citation instructions (link here)

Other finalised MEASO Biota pages provide good examples of how to populate these assessments.

MEASO Assessment pages should be titled: MEASO Biota: Species name/group

The purpose of these assessment pages is to summarise basic information for a species or taxonomic group and how the status and ecology of the group may be changing over time (link here to the framework for assessing biota within the MEASO framework). Authors are encouraged to use the partitioning of the marine ecosystem assessment (sectors etc - link here) as well as circumpolar information. Assessments of change can include historical change, current trends and/or prognoses for future change. Ideally, assessments will be quantitative but can include qualitative statements as well. Estimates of error and points of critical uncertainty need to be identified where possible.

Final assessments need to be written concisely, well-referenced, and using the uncertainty language of the IPCC. In the first instance, references can be from peer-reviewed literature, reports that are publicly available or references in the grey literature that could be obtained from repositories.

Under each heading is a list of information (in red italics) that is desirable for that section. Please do not change these main headings. If needed, a section can be further subdivided. Please delete the red italics and this window from the page when you have completed it (when the page is in edit mode you can select it for deletion).

Other finalised MEASO Biota pages provide good examples of how to populate these assessments.


Description

The shearwater profile covers short-tailed shearwaters (Ardenna tenuirostris) and sooty shearwaters (Ardenna griseus). These two species breed on southern hemisphere continents and forage in the Southern Ocean during the Austral summer before migrating to the northern hemisphere for the boreal summer.  


Taxonomy

Both species were previously within the genus Puffinus but this genus was split based on the results of a phylogenetic analysis of mitochondrial DNA by Penhallurick et al. (2004). 

Short-tailed shearwater: Animalia, Chordata, Aves, Procellariiformes, Procellariidae, Ardenna tenuirostris 

Sooty Shearwaters: Animalia, Chordata, Aves, Procellariiformes, Procellariidae, Ardenna grisea

(Note that on WoRMS Adrenna tenuirostris and Ardenna grisea are still unaccepted taxa, last checked 21/10/2019). 


Image: Short-tailed shearwater flying, www.nzbirdsonline.org.nz 

Image: Sooty shearwater on nest, Marcus Salton



Summary role in ecosystem


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Autecology


Life history

Parameters

Short-tailed

Sooty

Maximum age

Max age of short-tailed shearwaters is 38 years old, with the average age being 15 – 19 years old (Marshall and Serventy 1956).

Max age of sooty shearwaters is 30 years old with the average age around 17-20 years old (Warham et al. 1982).

Average adult size



Age at maturity

Short-tailed shearwaters reach maturity at 4-15 years of age, mean age for males = 7.3 years, mean age for females = 7.0 years (Skira 1991).

Sooty shearwaters reach maturity at a mean age of 6 years old (Richdale 1963).

Size at maturity

At age Short-tailed shearwaters weigh between 450 – 700 grams, have a total length of 43cm and wing span of one metre (Marshall and Serventy 1956).

At age sooty shearwaters weigh around 650 - 850 grams, reach a length 45- 50cm and have a wing span about one metre (Warham et al. 1982).

Spawning/breeding area

Burrows are located on headlands or islands (Skira et al. 1996).

Burrows are located on headlands or islands (Warham et al. 1982).  

Spawning/breeding season

Mating occurs in late October. Which is then followed by a 2 week exodus by the birds to put on weight for the egg laying period (Skira 1991).

Mating occurs in late October (Richdale 1963).

Larval/gestation period

Eggs laid from November 19 – December 2. The single egg is incubated for 52 – 55 days (Serventy 1963). Both parents incubate the egg for 10-16 days with males usually taking the first shift(Skira 1991). The majority of chicks hatch on 10th – 23rd of January (Oka et al. 1987).

Eggs are laid between November 16 and December 2 with the majority of eggs laid from November 20 - 24. The single egg is incubated for 53 days. Both parents incubate the egg for about 10 days with males usually taking the first shift. The majority of chicks hatch on 11th – 16th of January (Richdale 1963). 

Location of recruits

Recruits are based at the colony until fledging. Chicks begin to fledge about 4 months after hatching (Skira 1991).  

Based at the colony until fledging. Chicks fledge after 86 - 106 days after birth (Richdale 1963).

Size of recruits

Chicks (88 – 108 days old) attain a maximum mean weight of 800g nearly double that of adults (Skira 1991). This weight is then lost when chicks begin to fly.

Chicks (88 – 108 days old) attain a mean weight of 746g with a range of 570g – 922g (Warham et al. 1982)
Overall natural mortality rate

Non-predation natural mortality rates

Natural mortality generally occurs during the first migration due to starvation and exhaustion. The mortality rate of first year short-tailed shearwaters is 52% (Skira 1991).

Highest mortality rates in sooty shearwaters occurs in the first year of migration (Warham et al. 1982).


Migration, movement

Short-tailed Shearwater:

 

Each year millions of short-tailed shearwaters migrate from their breeding grounds in south eastern Australia to the North Pacific feeding grounds in the austral winter. There has been no direct migration pattern described for the short-tailed shearwater. However is has been acknowledged that the short-tailed shearwater flies about 15,000 kilometres annually in each direction (Serventy 1963). Short-tailed shearwaters have been known to fly this distance in 6 weeks (Serventy 1963).


Sexually immature birds are the first to migrate northwards departing at the end of March. Around mid-April breeding birds migrate northwards followed by fledged chick that leave around the end of April or early May. Short-tailed shearwaters being to arrive in North Pacific Ocean between the end of May and the beginning of June (Skira 1991).

Due to the presence of short-tailed shearwaters along the coasts of North America and Japan Serventy (1953) proposed that this species of seabird migrates in a figure of eight pattern. However in contrast to this, seabird surveys have reported that short-tailed shearwaters migrate across the Pacific Ocean broadly with many birds being sighted in the western sector of the Pacific (Skira 1991). It is clear that the movement between the two hemispheres by short-tailed shearwater is on a very broad front irrespective of its route. The route followed is likely to be determined by the age or a specific behaviour of the bird (Skira 1991).

Short-tailed shearwaters start to leave the northern hemisphere in late August early September however some birds may remain in the northern hemisphere for their first boreal winter (Marshall & Serventy 1956). Short-tailed shearwater begin to arrive to their breeding colonies by late September and early October (Skira 1991).

Mid-way through April adult sooty shearwaters begin to depart on their migration northwards to foraging grounds in the northern hemisphere. In the first week of May chicks begin to migrate north also. Sooty shearwaters undertake their migration to one of three areas in the western, central or eastern North Pacific (Hedd et al. 2012).

Sooty shearwaters are known to have a figure eight pattern migration which consists of covering a 64,000km, the longest animal migration to be recorded electronically (Hedd et al. 2012). Sooty shearwaters cover the entire Pacific Ocean during migration. Sooty shearwaters begin to return to their breeding colonies in the southern hemisphere in the first week of September (Hedd et al. 2012). 

Diet (foraging and consumption)

Short-tailed Shearwater:

Whilst feeding short-tailed shearwaters form large aggregations on the surface of the water known as ‘rafts’. These rafts are most commonly found in calm weather and usually occur when feeding or resting (Skira 1991). Short-tailed shearwaters have been found as deep 20m in the water column chasing prey (Weimerskirch & Sagar 1996). The most common foraging techniques used by short-tailed shearwaters are pursuit plunging, surface seizing, pursuit diving, scavenging and bottom feeding (Skira 1991).

Parental short-tailed shearwaters use a 2 fold foraging strategy to feed their chicks (Weimerskirch & Cherel 1998). Parents on average preform 2 successive 1 – 2 day short trips to gather food followed by a long trip (9 – 17 days). Decisions whether to forage in close or distant waters is dependent on the body condition of the parent. Birds with poor body condition are likely to go on long trips to rich areas of food (e.g. Polar Frontal Zone) whereas those in good condition continue to forage in waters close to their breeding colonies (Weimerskirch & Cherel 1998).

In the southern hemisphere the main prey items are the krill Nyctiphanes australis, arrow squid Notodarus sloani gouldi, other squid, fish and crustaceans (Montague et al. 1986; Skira 1986). However the diet of short-tailed shearwaters changes from a krill dominated diet to a mixture of fish, squid and crustaceans once the eggs hatch in January (Montague et al. 1986). During the non-breeding period in the northern hemisphere crustaceans (euphausiids and amphipods) fish and occasionally cephalopod make up the diet of short-tailed shearwater (Shaffer et al. 2006).

On their long trips south, South Australian short-tailed shearwaters mainly forage from 110˚E - 150˚E at the Polar Front with the highest concentrations of birds being at 140˚E. These South Australian birds also forage south of the Polar Front with a distribution as far as 55˚E being recorded in waters at the southern boundary of the Antarctic Circumpolar Current 64˚S (Raymond et al. 2010).  Tasmanian short-tailed shearwaters consistently forage at the Polar Front at 165˚E and then forage in an east to west direction and returning to their colonies in and north east direction (Raymond et al. 2010).

Sooty Shearwater:

Sooty Shearwaters mainly use surface diving as their foraging technique but they also regularly plunge dive (Brown et al. 1981). Sooty shearwaters are able to compress their tarsus and narrow their pelvis which are favourable features for diving (Weimerskirch & Sagar 1996). Sooty shearwaters have been recorded to dive to depths up to 60m (Weimerskirch & Sager 1996). With a swimming speed of 2m per second (Swennen & Duiven 1991) shearwaters may remain submerged for up to a minute. Shearwaters dive down in a zigzag pattern to reduce buoyancy (Weimerskirch &Sagar 1996). Reaching greater depths (as sooty shearwaters do) reduces the cost of diving (Weimerskirch & Sagar 1996).

The sooty shearwater has a highly variable diet. Whilst in the northern hemisphere the sooty shearwater diet consists of anchovies Engraulis species, juvenile rockfish Sebastes species, market squid Loligo opalescens and small fishes such as capelinMollotus villosus and sandlance  Ammodytidae (Brown et al 1981; Chu 1984; Shiomi & Ogi 1992).

In the southern hemisphere the diet of sooty shearwaters is highly dominated by crustacean. The main prey species of the sooty shearwater in the southern hemisphere are the euphausiids Euphausia and Nyctiphanes, the amphipods Hyperia andParathemisto, the salp Pyrosoma and the fishes Maurolicus and Sprattus (Raymond et al. 2010). Sooty shearwaters from New Zealand travel to two main foraging locations (160˚E and 140˚E) at the Polar Frontal Zone (Raymond et al. 2010).

Energetics


Parameters

Short-tailed

Sooty
Ingestion rateInsert values and short citations here
Metabolism

Fecundity

One egg is laid and no relaying occurs if egg is lost (Skira 1991).

One egg is laid and no relaying occurs if egg is lost (Richdale 1963).

Length-weight relationships



Growth rate



Size at age

At age Short-tailed shearwaters weigh between 450 – 700 grams, have a total length of 43cm and wing span of one metre (Marshall and Serventy 1956).  

At age sooty shearwaters weigh around 650 - 850 grams, reach a length 45- 50cm and have a wing span about one metre (Warham et al. 1982).
Population Productivity (average life time)

Habitat


Short-tailed shearwater: 

Short-tailed shearwaters are usually found on headlands and small islands during the breeding season. Headlands allow for easy take-off and landing for these birds (Serventy 1953). Their burrows are found far from land foraging. Suitable soil for burrows or rock crevices are required for suitable nests (Warham et al. 1982).  

Sooty shearwater:

Sooty shearwater colonies are found on headlands and small offshore islands. However in the non-breeding season sooty shearwaters are found far from land. Suitable soil for burrows or rock crevices are required for suitable nests (Warham et al. 1982).

Relationships, thresholds and limits

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Observed or expected functional responses to different drivers

Here we ask that you endeavour to characterise the relationships of the taxon with the habitat as a function relationship, i.e. the response of the taxon (life stage)(y-axis) relative to the magnitude of the habitat (x-axis).  We provide icons below to paste into the table.  If possible, add the values of the parameters of the relationship and detail the uncertainty around them.

 

VariableTaxon size/stage impactedFunctional response (icon)Parameters and uncertaintiesRisk areas/regions impactedNotes



Paste icon here
















Population



Short-tailed and sooty shearwater represent two of the most abundant species of shearwaters globally. 

Short-tailed shearwater: 

Estimated global population >23 million individuals (Brooke, 2004). 

Sooty shearwater: 

Global population estimated at 4.4 million pairs, roughly equating to 19.0-23.6 million individuals (Newman et al. 2009, Waugh et al. 2013). 

Range and Structure

Short-tailed shearwater: 

The short-tailed shearwater is a migratory species that moves between breeding colonies in south-eastern Australia and foraging grounds in the North Pacific Ocean. Main breeding grounds are found in South Australia, eastern New South Wales and eastern Tasmania. Short tailed Shearwaters can be found as southward as the Antarctic continent foraging in the Austral summer (Weimerskirch & Cherel 1998).  

 It has been estimated that there are twenty three million short-tailed shearwaters globally, making them a highly important part of the Southern Ocean ecosystem (Weimerskirch & Cherel 1998). Short-tailed shearwater breed in about 285 colonies in south-eastern Australia (Skira 1991). Approximately eighteen million of these seabirds arrive in Tasmanian each year where there are 167 known colonies with an estimated eleven million burrows (Skira 1991).

Sooty shearwater: 

The sooty shearwater is also a migratory species that breeds in the southern hemisphere, predominately on the coast of New Zealand with colonies also in Southern Australia, Tierra del Fuego, Chile and the Falkland Islands during the austral summer (Briggs & Chu 1986). As the austral winter approaches the sooty shearwaters migrate to the northern hemisphere feeding grounds where they can be found as far as Greenland in the Atlantic Ocean and Alaska in the Pacific Ocean (Phillips 1963).

It has been well documented that there is an increasing decline in sooty shearwater numbers (Jones 2000; Scofield & Christie 2002; Scott et al. 2008). While the decline has yet to be quantified it is likely the decline will have significant impacts on marine ecosystems. The decline of this seabird species has be attributed by fisheries,  seabird by-catch, global warming and introduced species on islands.


Latest static map of distribution if available

Relative abundance in different sectors (importance of different sectors to the group)




Dynamics

Short-tailed shearwater: 

Sooty shearwater:



Abundance information - general overview, comment on increases or decreases in population size and where/why?


Placeholder for trends in abundance in different sectors



Synecology



Consumers (predators)

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Competitors

Compete for food with pink salmon (Oncorhynchus gorbuscha) outside of Antarctica (Toge et al. 2011). 

Other interactions e.g. disease

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Human Impacts


Engtanglement

Harvesting

Ingestion of marine debris

Light Pollution 


Assessments of Status


IUCN Red List

Add the following table or simply say 'None of these species has been assessed for the Red List'

Species:Short-tailed shearwaterSooty shearwater
Year of classification:20182018
Red List Category & Criteria:Least concernNear threatened
Trend: 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.This species is classified as Near Threatened because it is thought to have undergone a moderately rapid decline owing to the impact of fisheries, the harvesting of its young and possibly climate change.
Assessment Justification: BirdLife International 2018. Ardenna tenuirostris. The IUCN Red List of Threatened Species 2018: e.T22698216A132635686. http://dx.doi.org/10.2305/IUCN.UK.2018-2.RLTS.T22698216A132635686.enDownloaded on 17 May 2019.

BirdLife International 2018. Ardenna griseaThe IUCN Red List of Threatened Species 2018: e.T22698209A132634513. http://dx.doi.org/10.2305/IUCN.UK.2018-2.RLTS.T22698209A132634513.enDownloaded on 17 May 2019.


Other

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References


A list of references referred to on this page.

Please use Ecology style, for more information and examples see: 

https://besjournals.onlinelibrary.wiley.com/hub/journal/13652745/author-guidelines

Briggs, K.T. & Chu, E.W. (1986) Sooty shearwaters off California: distribution, abundance and habitat use. The Condor, 88, 355-364.

Brown, R., Barker, S.P., Gaskin, D. & Sandeman, M.R. (1981) The foods of great and sooty shearwaters Puffinus gravis and P. griseus in eastern Canadian waters.Ibis, 123, 19-30.

Brooke, M. de. L. (2004). Albatrosses and Petrels Across the World. Oxford University Press, Oxford. 

Carey, M.J. (2011). Intergenerational transfer of plastic debris by Short-tailed Shearwaters (Ardenna tenuirostris). Emu-Austral Ornithology, 111, 229-234. Doi: 10.1071/MU10085

Chu, E. (1984) Sooty shearwaters off California: Diet and energy gain.

Clucas, R. (2011). Long‐term population trends of Sooty Shearwater (Puffinus griseus) revealed by hunt success. Ecological Applications, 21, 1308-1326. Doi: 10.1890/09-0813.1

DeGrange, A.R. & Day, R.H. (1991). Mortality of seabirds in the Japanese land-based gillnet fishery for salmon. The Condor 93, 251-258. Doi: 10.2307/1368940

Hedd, A., Montevecchi, W.A., Otley, H., Phillips, R.A. & Fifield, D.A. (2012) Trans-equatorial migration and habitat use by sooty shearwaters Puffinus griseus from the South Atlantic during the nonbreeding season. Marine Ecology Progress Series, 449, 277-290. Doi: 10.3354/meps09538

Waugh, S.M., Tennyson, A.J., Taylor, G.A. & Wilson, K.J. (2013). Population sizes of shearwaters (Puffinus spp.) breeding in New Zealand, with recommendations for monitoring. Tuhinga, 24, 159-204.

Jones, C. (2000). Sooty shearwater (Puffinus griseus) breeding colonies on mainland South Island, New Zealand: evidence of decline and predictors of persistence. New Zealand Journal of Zoology, 27, 327-334. Doi: 10.1080/03014223.2000.9518242

Marshall, A.J. & Serventy, D.L. (1956) The breeding cycle of the short-tailed shearwater, Puffinus tenuirostris, in relation to trans-equatorial migration and it’s environment. Proceedings of the Zoological Society of London, 489-510.

Montague, T., Cullen, J. & Fitzherbert, K. (1986) The diet of the short-tailed shearwater Puffinus tenuirostris during its breeding season. Emu, 86, 207-213.

Newman, J., Scott, D., Bragg, C., McKechnie, S., Moller, H. & Fletcher, D. (2009). Estimating regional population size and annual harvest intensity of the sooty shearwater in New Zealand. New Zealand Journal of Zoology, 36, 307-323. Doi: 10.1080/03014220909510157

Oka, N., Maruyama, N. & Skira, I. (1987) Chick growth and mortality of short-tailed shearwaters in comparison with sooty shearwaters, as a possible index of fluctuations of Australian krill abundance. Proceedings of the National Institute of Polar Research Symposium on Polar Biology, 1, 166-174.

Penhallurick, J. & Wink, M. (2004). Analysis of the taxonomy and nomenclature of the Procellariiformes based on complete nucleotide sequences of the mitochondrial cytochrome b gene. Emu, 104, 125-147. Doi: 10.1071/MU01060

Peter, J. & Dooley, S. (2014). The fatal shore. Australian Birdlife, 3, 24-27.

Phillips, J. (1963). The pelagic distribution of the sooty shearwater Procellaria grisea. Ibis, 105, 340-353.

Raymond, B., Shaffer, S.A., Sokolov, S., Woehler, E.J., Costa, D.P., Einoder, L., ... Sagar, P.M. (2010). Shearwater foraging in the Southern Ocean: the roles of prey availability and winds. PLoS One, 5, e10960. Doi: 10.1371/journal.pone.0010960

Richdale, L.E. (1963). Biology of the sooty shearwater Puffinus griseus. Proceedings of the Zoological Society of London, 1-117.

Scofield, R.P. & Christie, D. (2002). Beach patrol records indicate a substantial decline in sooty shearwater (Puffinus griseus) numbers. Notornis, 49, 158-165.

Scott, D., Scofield, P., Hunter, C. & Fletcher, D. (2008). Decline of Sooty Shearwaters, Puffinus griseus, on The Snares, New Zealand. Papers and Proceedings of the royal Society of Tasmania, 142, 185-196. Doi: 10.26749/rstpp.142.1.185

Serventy, D.L. (1953). Movements of pelagic sea-birds in the Indo-Pacific region. Seventh Pacific Science Congress of the Pacific Science Association: 394-406.

Serventy, D.L. (1963). Egg-laying timetable of the Slender-billed Shearwater, Puffinus tenuirostris. Proceedings of the 13th International Ornithological Congress, 338 – 343.

Shaffer, S.A., Tremblay, Y., Weimerskirch, H., Scott, D., Thompson, D.R., Sagar, P.M., ... Block, B.A. (2006). Migratory shearwaters integrate oceanic resources across the Pacific Ocean in an endless summer. Proceedings of the National Academy of Sciences, 103, 12799-12802. Doi: 10.1073/pnas.0603715103

Shiomi, K. & Ogi, H. (1992). Feeding ecology and body size dependence on diet of the sooty shearwater, Puffinus griseus, in the North Pacific. Proceedings of the National Institute of Polar Research Symposium on Polar Biology, 5, 105-113.

Skira, I. (1986). Food of the Short-Tailed Shearwater, Puffinus-Tenuirostris, in Tasmania. Wildlife Research, 13, 481-488.

Skira, I. (1991). The short-tailed shearwater: a review of its biology. Corella, 15, 45-52.

Swennen, C. & Duiven, P. (1991). Diving speed and food-size selection in common guillemots Uria aalgae. Netherlands Journal of Sea Research, 27, 191-196.                            

Toge, K., Yamashita, R., Kazama, K., Fukuwaka, M., Yamamura, O. & Watanuki, Y. (2011). The relationship between pink salmon biomass and the body condition of short-tailed shearwaters in the Bering Sea: can fish compete with seabirds? Proceedings of the Royal Society B: Biological Sciences, 278, 2584-2590. Doi: 10.1098/rspb.2010.2345

Uhlmann, S. (2003). Fisheries bycatch mortalities of sooty shearwaters (Puffinus griseus) and short-tailed shearwaters (P. tenuirostris) (p. 52). Wellington, New Zealand: Department of Conservation.

Warham, J., Wilson, G. & Keeley, B. (1982). The annual cycle of the sooty shearwater Puffinus griseus at the Snares Islands, New Zealand. Notornis, 29, 269-292.

Waugh, S.M., Tennyson, A.J., Taylor, G.A. & Wilson, K.J. (2013). Population sizes of shearwaters (Puffinus spp.) breeding in New Zealand, with recommendations for monitoring. Tuhinga, 24, 159-204.

Weimerskirch, H. & Cherel, Y. (1998). Feeding ecology of short-tailed shearwaters: breeding in Tasmania and foraging in the Antarctic? Marine Ecology Progress Series, 167, 261-274. Doi: 10.3354/meps167261

Weimerskirch, H. & Sagar, P. (1996). Diving depths of sooty shearwaters Puffinus griseus. Ibis, 138, 786-788. Doi: 10.1111/j.1474-919X.1996.tb08837.x

People


Contributing authors

NameAffiliation
Ben Morrisby
Jess-Melbourne ThomasAAD
Madeleine BrasierIMAS/ACE CRC

Version history

 Version number

Date of creation *

Expert reviewers

Peer reviewers

Date of completion*

1.02019.05.06












* Date format is YYYY.MM.DD

 

Citation