Marine Biology

, Volume 160, Issue 10, pp 2755–2762 | Cite as

Transatlantic migration by post-breeding puffins: a strategy to exploit a temporarily abundant food resource?

  • Mark J. Jessopp
  • Michelle Cronin
  • Thomas K. Doyle
  • Mark Wilson
  • Abigail McQuatters-Gollop
  • Stephen Newton
  • Richard A. Phillips
Original Paper

Abstract

The distribution of Atlantic puffins (Fratercula arctica) from Skellig Michael, south-west Ireland, was investigated using geolocation loggers between the 2010 and 2011 breeding seasons. All tracked birds travelled rapidly west into the North Atlantic at the end of the breeding season in August, with the majority undertaking transatlantic trips from Ireland to the Newfoundland-Labrador shelf. The furthest distance from the colony reached by each bird was not influenced by body mass or sex and was achieved in approximately 20 days. By October, all birds had moved back to the mid Atlantic where they remained resident until returning to the breeding colony. The most parsimonious explanation for the rapid, directed long-distance migration is that birds exploit the seasonally high abundance of prey [e.g., fish species such as capelin (Mallotus villosus) and sandlance (Ammodytes spp.)] off the Canadian coast, which is also utilised by large populations of North American seabirds at this time. Once the availability of this short-term prey resource has diminished, the tracked puffins moved back towards the north-east Atlantic. A relationship between relative abundance of puffins and zooplankton was found in all winter months, but after correcting for spatial autocorrelation, was only significant in November and January. Nevertheless, these results suggest a potential switch in diet from mainly fish during the breeding and early post-breeding periods to zooplankton over the remaining winter period. This study suggests that puffins from south-west Ireland have a long-distance migration strategy that is rare in breeding puffins from the UK and identifies a key non-breeding destination for puffins from Ireland. This has implications for the susceptibility of different breeding populations to the effects of possible climatic or oceanographic change.

References

  1. Anderson JT, Dalley EL, O’Driscoll RL (2002) Juvenile capelin (Mallotus villosus) off Newfoundland and Labrador in the 1990s. ICES J Mar Sci 59:917–928CrossRefGoogle Scholar
  2. Baillie SM, Jones IL (2003) Atlantic Puffin (Fratercula arctica) chick diet and reproductive performance at colonies with high and low capelin (Mallotus villosus) abundance. Can J Zool 81:1598–1607CrossRefGoogle Scholar
  3. Baillie SM, Jones IL (2004) Response of Atlantic puffins to a decline in capelin abundance at the Gannet Islands, Labrador. Waterbirds 27:102–111CrossRefGoogle Scholar
  4. Boertmann D (2011) Seabirds in the central North Atlantic, September 2006: further evidence for an oceanic seabird aggregation area. Mar Ornithol 39:183–188Google Scholar
  5. Broderick AC, Coyne MS, Fuller WJ, Glen F, Godley BJ (2007) Fidelity and over-wintering of sea turtles. Proc R Soc B Biol Sci 274:1533–1539CrossRefGoogle Scholar
  6. Brown JS, Laundré JW, Gurung M (1999) The ecology of fear: optimal foraging, game theory, and trophic interactions. J Mammal 80:385–399CrossRefGoogle Scholar
  7. Burke CM, Montevecchi WA (2008) Fish and chicks: forage fish and chick success in co-existing auks. Waterbirds 31:372–384CrossRefGoogle Scholar
  8. Carscadden J, Nakashima BS, Frank KT (1997) Effects of fish length and temperature on the timing of peak spawning in capelin (Mallotus villosus). Can J Fish Aquat Sci 54:781–787. doi:10.1139/f96-331 CrossRefGoogle Scholar
  9. Davis ND (1993) Caloric content of oceanic zooplankton and fishes for studies of salmonid food habits and their ecologically related species. (NPAFC Doc.) FRI-UW-9312. Fisheries Research Institute, University of Washington, SeattleGoogle Scholar
  10. Davoren GK (2007) Effects of gill-net fishing on marine birds in a biological hotspot in the Northwest Atlantic. Conserv Biol 21:1032–1045CrossRefGoogle Scholar
  11. Davoren GK, Anderson JT, Montevecchi WA (2006) Shoal behaviour and maturity relations of spawning capelin (Mallotus villosus) off Newfoundland: demersal spawning and diel vertical movement patterns. Can J Fish Aquat Sci 63:268–284CrossRefGoogle Scholar
  12. DFO (2011) Assessment of capelin in SA 2 + Div. 3KL in 2010. DFO Canadian Science Advisory Secretariat Science Advisory Report 2010/090Google Scholar
  13. Dias MP, Granadeiro JP, Phillips RA, Alonso H, Catry P (2011) Breaking the routine: individual Cory’s shearwaters shift winter destinations between hemispheres and across ocean basins. Proc R Soc B Biol Sci 278:1786–1793CrossRefGoogle Scholar
  14. Dutilleul P (1993) Modifying the t test for assessing the correlation between two spatial processes. Biometrics 49:305–314CrossRefGoogle Scholar
  15. Falk K, Jensen JK, Kampp K (1992) Winter diet of Atlantic puffins (Fratercula arctica) in the northeast Atlantic. Colon Waterbirds 15(2):230–235Google Scholar
  16. Fort J, Beaugrand G, Grémillet D, Phillips RA (2012) Biologging, remotely-sensed oceanography and the continuous plankton recorder reveal the environmental determinants of a seabird wintering hotspot. PLoS One 7:e41194CrossRefGoogle Scholar
  17. Frederiksen M, Moe B, Daunt F, Phillips RA, Barrett RT, Bogdanova MI, Boulinier T, Chardine JW, Chastel O, Chivers LS, Christensen-Dalsgaard S, Clément-Chastel C, Colhoun K, Freeman R, Gaston AJ, González-Solís J, Goutte A, Grémillet D, Guilford T, Jensen GH, Krasnov Y, Lorentsen SH, Mallory ML, Newell M, Olsen B, Shaw D, Steen H, Strøm H, Systad GH, Thórarinsson TL, Anker-Nilssen T (2012) Multicolony tracking reveals the winter distribution of a pelagic seabird on an ocean basin scale. Divers Distrib 18:530–542CrossRefGoogle Scholar
  18. Gaston AJ, Jones IL (1998) The auks. Oxford University Press, OxfordGoogle Scholar
  19. Guilford T, Meade J, Willis J, Phillips RA, Boyle D, Roberts S, Collett M, Freeman R, Perrins CM (2009) Migration and stopover in a small pelagic seabird, the Manx shearwater Puffinus puffinus: insights from machine learning. Proc R Soc B Biol Sci 276:1215–1223CrossRefGoogle Scholar
  20. Guilford T, Freeman R, Boyle D, Dean B, Kirk H, Phillips R, Perrins C (2011) A dispersive migration in the Atlantic puffin and its implications for migratory navigation. PLoS One 6:e21336CrossRefGoogle Scholar
  21. Haining R (1991) Bivariate correlation with spatial data. Geogr Anal 23:210–227CrossRefGoogle Scholar
  22. Harris MP, Wanless S (2011) The puffin. Poyser, LondonGoogle Scholar
  23. Harris M, Daunt F, Newell M, Phillips R, Wanless S (2010) Wintering areas of adult Atlantic puffins Fratercula arctica from a North Sea colony as revealed by geolocation technology. Mar Biol 157:827–836CrossRefGoogle Scholar
  24. Hedd A, Fifield DA, Burke CM, Montevecchi WA, Tranquilla LMF, Regular PM, Buren AD, Robertson GJ (2010) Seasonal shift in the foraging niche of Atlantic puffins Fratercula arctica revealed by stable isotope (δ 15N and δ 13 C) analyses. Aquat Biol 9:13–22CrossRefGoogle Scholar
  25. Hedd A, Montevecchi WA, Otley H, Phillips RA, Fifield DA (2012) Trans-equatorial migration and habitat use by sooty shearwaters Puffinus griseus from the South Atlantic during the nonbreeding season. Mar Ecol Prog Ser 449:277–290. doi:10.3354/meps09538 CrossRefGoogle Scholar
  26. Jorgensen SJ, Reeb CA, Chapple TK, Anderson S, Perle C, Van Sommeran SR, Fritz-Cope C, Brown AC, Klimley AP, Block BA (2010) Philopatry and migration of Pacific white sharks. Proc R Soc B Biol Sci 277:679–688CrossRefGoogle Scholar
  27. Landers TJ, Rayner MJ, Phillips RA, Hauber ME (2011) Dynamics of seasonal movements by a trans-Pacific migrant, the Westland petrel Procellaria westlandica. Condor 113:71–79CrossRefGoogle Scholar
  28. Lawson JW, Magalhães AM, Miller EH (1998) Important prey species of marine vertebrate predators in the northwest Atlantic: proximate composition and energy density. Mar Ecol Prog Ser 164:13–20CrossRefGoogle Scholar
  29. Lilliendahl K, Solmundsson J (1997) An estimate of summer food consumption of six seabird species in Iceland. ICES J Mar Sci 54:624CrossRefGoogle Scholar
  30. Lowther PE, Diamond AW, Kress SW, Robertson GJ, Russell K (2002) Atlantic puffin (Fratercula arctica). In: Poole A, Gill F (eds) Birds of North America. The Birds of North America Inc., PhiladelphiaGoogle Scholar
  31. Lyngs P (2003) Migration and winter ranges of birds in Greenland. Danish Ornithological Society, CopenhagenGoogle Scholar
  32. Mackley EK, Phillips RA, Silk JRD, Wakefield ED, Afanasyev V, Fox JW, Furness RW (2010) Free as a bird? Activity patterns of albatrosses during the nonbreeding period. Mar Ecol Prog Ser 406:291–303CrossRefGoogle Scholar
  33. McFarlane Tranquilla L, Hedd A, Burke C, Montevecchi WA, Regular PM, Robertson GJ, Stapleton LA, Wilhelm SI, Fifield DA, Buren AD (2010) High Arctic sea ice conditions influence marine birds wintering in low Arctic regions. Estuar Coast Shelf Sci 89:97–106CrossRefGoogle Scholar
  34. Meinertzhagen R (1955) The speed and altitude of bird flight. Ibis 78:81–117Google Scholar
  35. Mitchell PE, Newton SF, Ratcliffe N, Dun TE (2004) Seabird populations of Britain and Ireland. Results of the seabird 2000 census (1998–2002). A&C Black publishers Ltd, LondonGoogle Scholar
  36. Montevecchi W, Hedd A, McFarlane Tranquilla L, Fifield D, Burke C, Regular P, Davoren G, Garthe S, Robertson G, Phillips R (2012) Tracking seabirds to identify ecologically important and high risk marine areas in the western North Atlantic. Biol Conserv 156:62–71CrossRefGoogle Scholar
  37. Newton I (2010) Bird migration, vol 113. HarperCollins, UKGoogle Scholar
  38. Pennycuick C (1997) Actual and ‘optimum’ flight speeds: field data reassessed. J Exp Biol 200:2355–2361Google Scholar
  39. Phillips R, Silk J, Croxall J, Afanasyev V, Briggs D (2004) Accuracy of geolocation estimates for flying seabirds. Mar Ecol Prog Ser 266:265–272CrossRefGoogle Scholar
  40. Pitois SG, Fox CJ (2006) Long-term changes in zooplankton biomass concentration and mean size over the Northwest European shelf inferred from continuous plankton recorder data. ICES J Mar Sci J du Conseil 63:785–798CrossRefGoogle Scholar
  41. Pyke GH (1978) Optimal foraging: movement patterns of bumblebees between inflorescences. Theor Popul Biol 13:72–98CrossRefGoogle Scholar
  42. Richardson A, Walne A, John A, Jonas T, Lindley J, Sims D, Stevens D, Witt M (2006) Using continuous plankton recorder data. Prog Oceanogr 68:27–74CrossRefGoogle Scholar
  43. Rodway M, Montevecchi W (1996) Sampling methods for assessing the diets of Atlantic puffin chicks. Mar Ecol Prog Ser 144:41–55CrossRefGoogle Scholar
  44. Rosenberg MS, Anderson CD (2011) PASSaGE: pattern analysis, spatial statistics and geographic exegesis. Version 2. Methods Ecol Evol 2:229–232CrossRefGoogle Scholar
  45. Shaffer SA, Tremblay Y, Weimerskirch H, Scott D, Thompson DR, Sagar PM, Moller H, Taylor GA, Foley DG, Block BA (2006) Migratory shearwaters integrate oceanic resources across the Pacific Ocean in an endless summer. Proc Natl Acad Sci 103:12799CrossRefGoogle Scholar
  46. Spitz J, Mourocq E, Schoen V, Ridoux V (2010) Proximate composition and energy content of forage species from the Bay of Biscay: high-or low-quality food? ICES J Mar Sci J du Conseil 67:909–915CrossRefGoogle Scholar
  47. Steimle F, Terranova RJ (1985) Energy equivalents of marine organisms from the continental shelf of the temperate northwest Atlantic. J Northwest Atl Fish Sci 6:117–124CrossRefGoogle Scholar
  48. Storer RW (1960) Evolution of the diving birds. Proceedings 12th International Ornithological Congress, pp 55–70Google Scholar
  49. Sydeman WJ, Thompson SA, Santora JA, Henry MF, Morgan KH, Batten SD (2010) Macro-ecology of plankton–seabird associations in the North Pacific Ocean. J Plankton Res 32:1697–1713CrossRefGoogle Scholar
  50. Underwood L, Stowe T (1984) Massive wreck of seabirds in eastern Britain, 1983. Bird Study 31:79–88CrossRefGoogle Scholar
  51. Vandenabeele S, Shepard E, Grogan A, Wilson R (2012) When three per cent may not be three per cent; device-equipped seabirds experience variable flight constraints. Mar Biol 159:1–14CrossRefGoogle Scholar
  52. Wakefield ED, McFarlane-Tranquilla LA, Hedd A, Phillips RA, Montevecchi WA, Aebischer A, Bogdanova MI, Boulinier T, Bried J, Catry P, Cuthbert RJ, Daunt F, Dias MP, Egevang C, Freeman R, Furness RW, Gaston AJ, Geraldes P, Gilg O, González-Solís J, Granadeiro JP, Gremillet D, Guilford T, Hahn S, Hamer KC, Kolbeinsson Y, Kopp M, Magalhães MC, Magnusdottir E, Militão T, Moe B, Neves V, Paiva VP, Peter HU, Petersen AE, Quinn LR, Ramirez I, Ramos R, Ramsay A, Ryan PG, Serrão Santos RS, Sigurõsson IA, Sittler B, Stenhouse IJ, Thompson PM, Witt MJ (2011) A newly described seabird diversity hotspot in the deep Northwest Atlantic identified using individual movement data Seabird Group, 11th International Conference, Plymouth, UK. http://www.seabirdgroup.org.uk/?page=conference
  53. Wilson RP, Hustler K, Ryan PG, Burger AE, Noldeke EC (1992) Diving birds in cold water: do Archimedes and Boyle determine energetic costs? Am Nat 140:179–200CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2013

Authors and Affiliations

  • Mark J. Jessopp
    • 1
  • Michelle Cronin
    • 1
  • Thomas K. Doyle
    • 1
  • Mark Wilson
    • 2
  • Abigail McQuatters-Gollop
    • 3
  • Stephen Newton
    • 4
  • Richard A. Phillips
    • 5
  1. 1.Coastal and Marine Research Centre, Environmental Research InstituteUniversity College CorkCorkIreland
  2. 2.School of Biological, Earth and Environmental ScienceUniversity College CorkCorkIreland
  3. 3.Sir Alistair Hardy Foundation for Ocean SciencePlymouthUK
  4. 4.Birdwatch IrelandKilcooleIreland
  5. 5.British Antarctic SurveyNatural Environment Research CouncilCambridgeUK

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