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European Journal of Wildlife Research

, Volume 58, Issue 1, pp 255–267 | Cite as

Low survival after release into the wild: assessing “the burden of captivity” on Mallard physiology and behaviour

  • Jocelyn ChampagnonEmail author
  • Matthieu Guillemain
  • Johan Elmberg
  • Grégoire Massez
  • Francois Cavallo
  • Michel Gauthier-Clerc
Original Paper

Abstract

Captive-reared animals used in reinforcement programs are generally less likely to survive than wild conspecifics. Digestion efficiency and naive behaviour are two likely reasons for this pattern. The Mallard is a species with high adaptability to its environment and in which massive reinforcement programs are carried out. We studied physiological and behavioural factors potentially affecting body condition and survival of captive-reared Mallards after being released. Digestive system morphology and an index of body condition were compared among three groups: captive-reared birds remaining in a farm (control), captive-reared birds released into the wild as juveniles (released) and wild-born birds (wild). We also compared behaviour and diet of released vs. wild Mallards. Finally, we conducted a 1-year survival analysis of captive-reared birds after release in a hunting-free area. Gizzard weight was lower in control Mallards, but the size of other organs did not differ between controls and wild birds. The difference in gizzard weight between released and wild birds disappeared after some time in the wild. Diet analyses suggest that released Mallards show a greater preference than wild for anthropogenic food (waste grain, bait). Despite similar time-budgets, released Mallards never attained the body condition of wild birds. As a consequence, survival probability in released Mallards was low, especially when food provisioning was stopped and during harsh winter periods. We argue that the low survival of released Mallards likely has a physiological rather than a behavioural (foraging) origin. In any case, extremely few released birds live long enough to potentially enter the breeding population, even without hunting. In the context of massive releases presently carried out for hunting purposes, our study indicates a low likelihood for genetic introgression by captive-reared birds into the wild population.

Keywords

Anas platyrhynchos Digestive system E-SURGE Nasal saddle Scaled mass index Restocking 

Notes

Acknowledgements

The control Mallards were sacrificed in conformity with the French legal requirement by Elevage Bravo (FR 30-033-111 CE). We are grateful to Marais du Vigueirat and Vincent Milla (Elevage des Courrèges) to let us conduct this experiment with their collaboration, the Centre de Recherche sur la Biologie des Populations d’Oiseaux (Muséum National d’Histoire Naturelle, Paris) for providing rings and Quentin Charel for preparing the nasal saddles. We thank all hunters who sent back rings and all landowners and game keepers who provided Mallards from hunting bags: Mr. Herbinger and Mr. Aubert, Mr. Nourry, Mr. Sire, Mr. Razier and Mr. Cordesse. Dissection was performed by Mathieu Famette, and JC. Jean-Baptiste Mouronval, Mathieu Famette and Antony Marchet identified seeds in gut contents. Additional field observations of marked birds were provided by Fanny Rey, Charlène Stewart, Adrien Raggiotto, Aude Pouyès, Aurélien Villard and Sylvain Ceyte. We thank Jean-Dominique Lebreton and Jean-Baptiste Mouronval for comments that greatly helped in preparing the manuscript. This work was partially funded by the French “Agence Inter-établissement pour la Recherche et le Développement”. JE’s participation was supported by grant V-205-09 from the Swedish Environmental Protection Agency.

References

  1. Aaltonen K, Bryant AA, Hostetler JA, Oli MK (2009) Reintroducing endangered Vancouver Island marmots: survival and cause-specific mortality rates of captive-born versus wild-born individuals. Biol Conserv 142:2181–2190. doi: 10.1016/j.biocon.2009.04.019 CrossRefGoogle Scholar
  2. Altmann J (1974) Observational study of behaviour: sampling methods. Behaviour 49:227–267PubMedCrossRefGoogle Scholar
  3. Anderson DR, Burnham KP (1999) General strategies for the analysis of ringing data. Bird Study 46:261–270CrossRefGoogle Scholar
  4. Arzel C, Elmberg J, Guillemain M, Legagneux P, Bosca F, Chambouleyron M, Lepley M, Pin C, Arnaud A, Schricke V (2007) Average mass of seeds encountered by foraging dabbling ducks in western Europe. Wildl Biol 13:328–336CrossRefGoogle Scholar
  5. Aznar J-C, Dervieux A, Grillas P (2003) Association between aquatic vegetation and landscape indicators of human pressure. Wetlands 23:149–160CrossRefGoogle Scholar
  6. Bellrose CF (1985) The adaptability of the mallard leads to its future. Proceedings of the Mallard Symposium, Bismarck, North DakotaGoogle Scholar
  7. Berthold P (2001) Bird migration: a general survey. Oxford University, OxfordGoogle Scholar
  8. Britt A, Iambana BR (2003) Can captive-bred Varecia variegata variegata adapt to a natural diet on release to the wild? Int J Primatol 24:987–1005CrossRefGoogle Scholar
  9. Brown JL, Collopy MW, Gott EJ, Juergens PW, Montoya AB, Hunt WG (2006) Wild-reared Aplomado falcons survive and recruit at higher rates than hacked falcons in a common environment. Biol Conserv 131:453–458. doi: 10.1016/j.biocon.2006.02.021 CrossRefGoogle Scholar
  10. Byers SM, Cary JR (1991) Discrimination of Mallard strains on the basis of morphology. J Wildl Manage 55:580–586CrossRefGoogle Scholar
  11. Champagnon J, Guillemain M, Gauthier-Clerc M, Lebreton J-D, Elmberg J (2009) Consequences of massive bird releases for hunting purposes: Mallard Anas platyrhynchos in the Camargue, southern France. Wildfowl Special Issue 2:192–201Google Scholar
  12. Champagnon J, Guillemain M, Elmberg J, Folkesson K, Gauthier-Clerc M (2010) Changes in Mallard Anas platyrhynchos bill morphology after thirty years of supplemental stocking. Bird Study 57:344–351CrossRefGoogle Scholar
  13. Chauvelon P (1998) A wetland managed for agriculture as an interface between the Rhône river and the Vaccarès lagoon (Camargue, France): transfers of water and nutrients. Hydrobiologia 373:181–191CrossRefGoogle Scholar
  14. Choquet R, Lebreton J-D, Gimenez O, Reboulet A-M, Pradel R (2009a) U-CARE: utilities for performing goodness of fit tests and manipulating capture–recapture data. Ecography 32:1071–1074CrossRefGoogle Scholar
  15. Choquet R, Rouan L, Pradel R (2009b) Program E-Surge: a software application for fitting multievent models. In: Thomson DL, Cooch EG, Conroy MJ (eds) Modeling demographic processes in marked populations. Springer, New York, pp 845–865CrossRefGoogle Scholar
  16. Dawson RD, Bortolotti GR (2000) Effects of hematozoan parasites on condition and return rates of American kestrels. Auk 117:373–380CrossRefGoogle Scholar
  17. Dehorter O, Tamisier A (1996) Wetland habitat characteristics for waterfowl wintering in Camargue, Southern France: implications for conservation. Rev Ecol 51:161–172Google Scholar
  18. Del Hoyo J, Elliott A, Sargatal J (1992) Handbook of the birds of the world, vol 1. Lynx Edicions, BarcelonaGoogle Scholar
  19. Devries JH, Citta JJ, Lindberg MS, Howerter DW, Anderson MG (2003) Breeding-season survival of mallard females in the prairie pothole region of Canada. J Wildl Manage 67:551–563CrossRefGoogle Scholar
  20. Drobney RD (1984) Effect of diet on visceral morphology of breeding wood ducks. Auk 101:93–98Google Scholar
  21. Dunn J, Diefenbach D, Hartman F (1995) Survival and recovery distribution of wild and captive-reared mallards. Transactions of the Northeast Section of the Wildlife Society 52:21–28Google Scholar
  22. Fajardo I, Babiloni G, Mira Y (2000) Rehabilitated and wild barn owls (Tyto alba): dispersal, life expectancy and mortality in Spain. Biol Conserv 94:287–295. doi: 10.1016/S0006-3207(00)00003-3 CrossRefGoogle Scholar
  23. Fog J (1964) Dispersal and survival of released mallards (Anas platyrhynchos L.). Dan Rev Game Biol 4:1–57Google Scholar
  24. Guay P-J, Iwaniuk AN (2008) Captive breeding reduces brain volume in waterfowl (Anseriformes). Condor 110:276–284CrossRefGoogle Scholar
  25. Guillemain M, Fritz H, Guillon N, Simon G (2002a) Ecomorphology and coexistence in dabbling ducks: the role of lamellar density and body length. Oikos 98:547–551CrossRefGoogle Scholar
  26. Guillemain M, Martin GR, Fritz H (2002b) Feeding methods, visual fields and vigilance in dabbling ducks (Anatidae). Funct Ecol 16:522–529CrossRefGoogle Scholar
  27. Guillemain M, Poisbleau M, Denonfoux L, Lepley M, Moreau C, Massez G, Leray G, Caizergues A, Arzel C, Rodrigues D, Fritz H (2007) Multiple tests of the effect of nasal saddles on dabbling ducks: combining field and aviary approaches. Bird Study 54:35–45CrossRefGoogle Scholar
  28. Guillemain M, Lepley M, Massez G, Caizairgues A, Rodrigues D, Figueiredo M (2008) Addendum: Eurasian Teal Anas crecca nasal saddle loss in the Camargue, France. Bird Study 55:135–138CrossRefGoogle Scholar
  29. Guillemain M, Elmberg J, Gauthier-Clerc M, Massez G, Hearn R, Champagnon J, Simon G (2010) Wintering French Mallard and Teal are heavier and in better body condition than 30 years ago: effects of a changing environment? Ambio 39:170–180PubMedCrossRefGoogle Scholar
  30. Gunnarsson G, Elmberg J, Dessborn L, Jonzén N, Pöysä H, Valkama J (2008) Survival estimates, mortality patterns, and population growth of Fennoscandian mallards Anas platyrhynchos. Ann Zool Fenn 45:483–495Google Scholar
  31. Hargrove JW, Borland CH (1994) Pooled population parameter estimates from mark-recapture data. Biometrics 50:1129–1141PubMedCrossRefGoogle Scholar
  32. Hart RK, Calver MC, Dickman CR (2002) The index of relative importance: an alternative approach to reducing bias in descriptive studies of animal diets. Wildl Res 29:415–421. doi: 10.1071/WR02009 CrossRefGoogle Scholar
  33. Havlin J (1991) Ringing results in hand-reared Anas platyrhynchos. Folia Zool 40:153–165Google Scholar
  34. Hestbeck JB, Dzubin A, Gollop JB, Nichols JD (1989) Mallard survival from local to immature stage in southwestern Saskatchewan. J Wildl Manage 53:428–431CrossRefGoogle Scholar
  35. Hodder K, Bullock J (1997) Translocations of native species in the UK: implications for biodiversity. J Appl Ecol 34:547–565CrossRefGoogle Scholar
  36. Jule KR, Leaver LA, Lea SE (2008) The effects of captive experience on reintroduction survival in carnivores: a review and analysis. Biol Conserv 141:355–363CrossRefGoogle Scholar
  37. Kayser Y, Gauthier-Clerc M, Béchet A, Poulin B, Massez G, Chérain Y, Paoli J, Sadoul N, Vialet E, Paulus G, Vincent-Martin N, Pilard P, Isenmann P (2008) Compte-rendu ornithologique camarguais pour les années 2001–2006. Rev Ecol 63:299–349Google Scholar
  38. Kehoe FP, Ankney CD, Alisauskas RT (1988) Effects of dietary fiber and diet diversity on digestive organs of captive mallards (Anas platyrhynchos). Can J Zool 66:1597–1602. doi: 10.1139/z88-233 CrossRefGoogle Scholar
  39. Krapu GL, Johnson DH, Dane CW (1979) Age determination of mallards. J Wildl Manage 43:384–393CrossRefGoogle Scholar
  40. Laikre L, Palmé A, Josefsson M, Utter F, Ryman N (2006) Release of alien populations in Sweden. Ambio 35:255–261PubMedCrossRefGoogle Scholar
  41. Laikre L, Schwartz MK, Waples RS, Ryman N, The GeM Working Group (2010) Compromising genetic diversity in the wild: unmonitored large-scale release of plants and animals. TREE 25:520–529PubMedGoogle Scholar
  42. Lambert E, Dutartre A, Coudreuse J, Haury J (2010) Relationships between the biomass production of invasive Ludwigia species and physical properties of habitats in France. Hydrobiologia 656:173–186CrossRefGoogle Scholar
  43. Latorre-Margalef N, Gunnarsson G, Munster VJ, Fouchier RA, Osterhaus AD, Elmberg J, Olsen B, Wallensten A, Haemig PD, Fransson T, Brudin L, Waldenström J (2009) Effects of influenza A virus infection on migrating mallard ducks. Proc R Soc Lond B 276:1029–1036CrossRefGoogle Scholar
  44. Le Gouar P, Robert A, Choisy J-P, Henriquet S, Lecuyer P, Tessier C, Sarrazin F (2008) Roles of survival and dispersal in reintroduction success of griffon vulture (Gyps fulvus). Ecol Appl 18:859–872PubMedCrossRefGoogle Scholar
  45. Lebreton J-D, Burnham KP, Clobert J, Anderson DR (1992) Modeling survival and testing biological hypotheses using marked animals: a unified approach with case studies. Ecol Monogr 62:67–118. doi: 10.2307/2937171 CrossRefGoogle Scholar
  46. Legagneux P, Inchausti P, Bourguemestre F, Latraube F, Bretagnolle V (2009) Effect of predation risk, body size, and habitat characteristics on emigration decisions in mallards. Behav Ecol 20:186–194CrossRefGoogle Scholar
  47. Liukkonen-Anttila T, Saartoala R, Hissa R (2000) Impact of hand-rearing on morphology and physiology of the Capercaillie (Tetrao urogallus). Comp Biochem Physiol A 125:211–221. doi: 10.1016/S1095-6433(99)00174-9 Google Scholar
  48. Martin TE (1987) Food as a limit on breeding birds: a life-history perspective. Ann Rev Ecol Syst 18:453–487CrossRefGoogle Scholar
  49. Mathews F, Orros M, McLaren G, Gelling M, Foster R (2005) Keeping fit on the ark: assessing the suitability of captive-bred animals for release. Biol Conserv 121:569–577CrossRefGoogle Scholar
  50. McWilliams SR, Karasov WH (2001) Phenotypic flexibility in digestive system structure and function in migratory birds and its ecological significance. Comp Biochem Physiol A 128:577–591CrossRefGoogle Scholar
  51. Moore SJ, Battley PF (2006) Differences in the digestive organ morphology of captive and wild Brown Teal Anas chlorotis and implications for releases. Bird Conserv Int 16:253–264. doi: 10.1017/S0959270906000396 CrossRefGoogle Scholar
  52. Mouronval J-B, Baudouin S (2010) Plantes aquatiques de Camargue et de Crau. Office National de la Chasse et de la Faune Sauvage, ParisGoogle Scholar
  53. Mouronval J-B, Guillemain M, Canny A, Poirier F (2007) Diet of non-breeding wildfowl Anatidae and Coot Fulica atra on the Perthois gravel pits, Northeast France. Wildfowl 57:68–97Google Scholar
  54. Musil DD, Connelly JW (2009) Survival and reproduction of pen-reared vs translocated wild pheasants Phasianus colchicus. Wildl Biol 15:80–88. doi: 10.2981/07-049 CrossRefGoogle Scholar
  55. Mysterud A (2010) Still walking on the wild side? Management actions as steps towards semi-domestication of hunted ungulates. J Appl Ecol 47:920–925CrossRefGoogle Scholar
  56. Naya DE, Bacigalupe LD, Bustamante DM, Bozinovic F (2005) Dynamic digestive responses to increased energy demands in the leaf-eared mouse (Phyllotis darwini). J Comp Physiol B 175:31–36PubMedCrossRefGoogle Scholar
  57. Newton I (2007) Weather-related mass-mortality events in migrants. Ibis 149:453–467CrossRefGoogle Scholar
  58. Nichols J, Hines JE (1993) Survival rate estimation in the presence of tag loss using joint analysis of capture–recapture and resighting data. In: Lebreton J-D, North P (eds) Marked individuals in the study of bird populations. Birkhäuser Verlag, Boston, pp 157–166Google Scholar
  59. O’Regan HJ, Kitchener AC (2005) The effects of captivity on the morphology of captive, domesticated and feral mammals. Mamm Rev 35:215–230CrossRefGoogle Scholar
  60. Parish DMB, Sotherton NW (2007) The fate of released captive-reared grey partridges Perdix perdix: implications for reintroduction programmes. Wildl Biol 13:140–149. doi: 10.2981/0909-6396 CrossRefGoogle Scholar
  61. Peig J, Green AJ (2009) New perspectives for estimating body condition from mass/length data: the scaled mass index as an alternative method. Oikos 118:1883–1891CrossRefGoogle Scholar
  62. Pinkas L, Oliphant M, Iverson I (1971) Food habits of albacore, bluefin tuna, and bonito in California waters. Fish Bull 152:11–105Google Scholar
  63. Pradel R (1993) Flexibility in survival analysis from recapture data: handling trap-dependence. In: Lebreton J-D, North P (eds) Marked individuals in the study of bird population. Birkhäuser Verlag, Boston, pp 29–37Google Scholar
  64. Putman RJ, Staines BW (2004) Supplementary winter feeding of wild red deer Cervus elaphus in Europe and North America: justifications, feeding practice and effectiveness. Mamm Rev 34:285–306CrossRefGoogle Scholar
  65. Roche EA, Cuthbert FJ, Arnold TW (2008) Relative fitness of wild and captive-reared piping plovers: does egg salvage contribute to recovery of the endangered Great Lakes population? Biol Conserv 141:3079–3088. doi: 10.1016/j.biocon.2008.09.014 CrossRefGoogle Scholar
  66. Santos T, Pérez-Tris J, Carbonell R, Tellería JL, Díaz JA (2009) Monitoring the performance of wild-born and introduced lizards in a fragmented landscape: implications for ex situ conservation programmes. Biol Conserv 142:2923–2930CrossRefGoogle Scholar
  67. Schladweiler JL, Tester JR (1972) Survival and behaviour of hand-reared mallards released in the wild. J Wildl Manage 36:1118–1127CrossRefGoogle Scholar
  68. Suter W, van Eerden MR (1992) Simultaneous mass starvation of wintering divingducks in Switzerland and the Netherlands: a wrong decision in the right strategy. Ardea 80:229–242Google Scholar
  69. Swanson G, Bartonek J (1970) Bias associated with food analysis in gizzards of blue-winged Teal. J Wildl Manage 34:739–746CrossRefGoogle Scholar
  70. Tamisier A, Dehorter O (1999) Camargue, canards et foulques. Centre Ornithologique du Gard, NîmesGoogle Scholar
  71. Tavecchia G, Pradel R, Lebreton J-D, Johnson AR, Mondain-Monval J-Y (2001) The effect of lead exposure on survival of adult mallards in the Camargue, southern France. J Appl Ecol 38:1197–1207CrossRefGoogle Scholar
  72. Tavecchia G, Viedma C, Martínez-Abraín A, Bartolomé M-A, Gómez JA, Oro D (2009) Maximizing re-introduction success: assessing the immediate cost of release in a threatened waterfowl. Biol Conserv 142:3005–3012. doi: 10.1016/j.biocon.2009.07.035 CrossRefGoogle Scholar
  73. Thomson DL, Conroy MJ, Anderson DR, Burnham KP, Cooch EG, Francis CM, Lebreton J-D, Lindberg MS, Morgan BJ, Otis DL, White GC (2009) Standardising terminology and notation for the analysis of demographic processes in marked populations. In: Thomson DL, Cooch EG, Conroy MJ (eds) Environmental and ecological statistics. Springer, New York, pp 1099–1106Google Scholar
  74. Tufto J (2001) Effects of releasing maladapted individuals: a demographic–evolutionary model. Am Nat 158:331–340. doi: 10.1086/321987 PubMedCrossRefGoogle Scholar
  75. Watkins EJ, Butler PJ, Kenyon BP (2004) Posthatch growth of the digestive system in wild and domesticated ducks. Br Poult Sci 45:331–341PubMedCrossRefGoogle Scholar
  76. Whyte RJ, Bolen EG (1984) Impact of winter stress on Mallard body composition. Condor 86:477–482CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • Jocelyn Champagnon
    • 1
    • 2
    • 3
    Email author
  • Matthieu Guillemain
    • 1
  • Johan Elmberg
    • 4
  • Grégoire Massez
    • 5
  • Francois Cavallo
    • 1
  • Michel Gauthier-Clerc
    • 2
  1. 1.Office National de la Faune SauvageCNERA Avifaune MigratriceArlesFrance
  2. 2.Centre de Recherche de la Tour du ValatArlesFrance
  3. 3.Centre d’Ecologie Fonctionnelle et Evolutive UMR 5175-CNRSMontpellier Cedex 5France
  4. 4.Aquatic Biology and ChemistryKristianstad UniversityKristianstadSweden
  5. 5.Les Marais du VigueiratArlesFrance

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