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A review of the nest protection hypothesis: does inclusion of fresh green plant material in birds’ nests reduce parasite infestation?

Published online by Cambridge University Press:  25 March 2015

JAMES F. SCOTT-BAUMANN  and
ERIC R. MORGAN
JAMES F. SCOTT-BAUMANN*
Affiliation:
School of Biological Sciences, University of Bristol, Life Sciences Building, 24 Tyndall Avenue, Bristol BS8 1TQ, UK
ERIC R. MORGAN
Affiliation:
School of Biological Sciences, University of Bristol, Life Sciences Building, 24 Tyndall Avenue, Bristol BS8 1TQ, UK
*
* Corresponding author: The Old Smithy, 3 Kent road, Congresbury, Somerset, BS49 5BD, UK. E-mail: [email protected]
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Summary

The use of aromatic plants and their essential oils for ectoparasite treatment is a field of growing interest. Several species of birds regularly introduce aromatic herbs into their nests putatively to reduce parasites. The behaviour is most often seen in cavity nesting birds and after nest building has finished. The plants are included in a non-structural manner and are often strongly aromatic. Various different hypotheses have been proposed regarding the function of this behaviour; from the plants altering some non-living factor in the nest (crypsis, water loss and insulation hypotheses) to them being involved in mate selection (mate hypothesis) or even having a beneficial effect, direct or indirect, on chicks (drug or nest protection hypothesis, NPH). Many studies have been carried out over the years observing and experimentally testing these hypotheses. This review focuses on studies involving the most popular of these hypotheses, the NPH: that plants decrease nest parasites or pathogens, thereby conveying positive effects to the chicks, allowing the behaviour to evolve. Studies providing observational evidence towards this hypothesis and those experimentally testing it are discussed.

Keywords

aromaticblue titstarlingnest protectionnesting material
Type
Review Article
Information
Parasitology , Volume 142 , Issue 8 , July 2015 , pp. 1016 - 1023
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Copyright
Copyright © Cambridge University Press 2015 

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References

REFERENCES

Bakkali, F., Averbeck, S., Averbeck, D. and Idaomar, M. (2008). Biological effects of essential oils–a review. Food and Chemical Toxicology : An International Journal Published for the British Industrial Biological Research Association 46, 446–475.CrossRefGoogle ScholarPubMed
Banbura, J., Blondel, J., Wilde-Lambrechts, H. and Perret, P. (1995). Why do female blue tits (Parus careuleus) bring fresh plants to their nests? Journal Für Ornithologie 136, 217–221.Google Scholar
Brouwer, L. and Komdeur, J. (2004). Green nesting material has a function in mate attraction in the European starling. Animal Behaviour 67, 539–548.Google Scholar
Christe, P., Richner, H. and Oppliger, A. (1996). Begging, food provisioning, and nestling competition in great tit broods infested with ectoparasites. Behavioral Ecology 7, 127–131.CrossRefGoogle Scholar
Clark, L. and Mason, J. (1985). Use of nest material as insecticidal and anti-pathogenic agents by the European starling. Oecologia 67, 169–176.Google Scholar
Clark, L. and Mason, J. (1988). Effect of biologically-active plants used as nest material and the derived benefit to starling nestlings. Oecologia 77, 174–180.Google Scholar
Clark, L. and Smeraski, C. A. (1990). Seasonal shifts in odor acuity by starlings. Journal of Experimental Zoology 255, 22–29.Google Scholar
Cowie, R. J. and Hinsley, S. A. (1988). Timing of return with green vegetation by nesting blue tits parus caeruleus. Ibis 130, 553–555.Google Scholar
Dawson, R. D. (2004). Does fresh vegetation protect avian nests from ectoparasites? An experiment with tree swallows. Canadian Journal of Zoology-Revue Canadienne De Zoologie 82, 1005–1010.Google Scholar
Dykstra, C. R., Hays, J. L. and Simon, M. M. (2009). Selection of fresh vegetation for nest lining by red-shouldered hawks. The Wilson Journal of Ornithology 121, 207–210.Google Scholar
Fauth, P., Krementz, D. and Hines, J. (1991). Ectoparasitism and the role of green nesting material in the European starling. Oecologia 88, 22–29.CrossRefGoogle ScholarPubMed
Feare, C. J. (1976). Desertion and abnormal development in a colony of sooty terns Sterna fuscata infested by virus-infected ticks. Ibis 118, 112–115.Google Scholar
De Groof, G., Gwinner, H., Steiger, S., Kempenaers, B. and Van der Linden, A. (2010). Neural correlates of behavioural olfactory sensitivity changes seasonally in European starlings. PLoS ONE 5 (12).Google Scholar
George, D. R., Callaghan, K., Guy, J. H. and Sparagano, O. A. E. (2008). Lack of prolonged activity of lavender essential oils as acaricides against the poultry red mite (Dermanyssus gallinae) under laboratory conditions. Research in Veterinary Science 85, 540–542.CrossRefGoogle Scholar
Goodenough, A. E., Elliot, S. L. and Hart, A. G. (2011). Do orientation-based differences in nestbox temperature cause differential ectoparasite load and explain patterns of nest-site selection and offspring condition in great tits? International Journal of Zoology 2011. Retrieved from http://dx.doi.org/10.1155/2011/514913.Google Scholar
Goodenough, A. and Stallwood, B. (2012). Differences in culturable microbial communities in bird nestboxes according to orientation and influences on offspring quality in great tits (parus Major). Microbial Ecology 63, 986–995.Google Scholar
Gwinner, H. (1997). The function of green plants in nests of European starlings (Sturnus vulgaris). Behaviour 134, 337–351.CrossRefGoogle Scholar
Gwinner, H. (2013). Volatile Compounds in Nest Herbs. In Chemical Signals in Vertebrates 12. (ed. East, M. L., Dehnhard, M.), p. 356. Springer, Berlin, Germany.Google Scholar
Gwinner, H. and Berger, S. (2005). European starlings: nestling condition, parasites and green nest material during the breeding season. Journal of Ornithology 146, 365–371.Google Scholar
Gwinner, H. and Berger, S. (2006). Parasite defence in birds: the role of volatiles. Acta Zoologica Sinica 52(Supplement), 280–283.Google Scholar
Gwinner, H. and Berger, S. (2008). Starling males select green nest material by olfaction using experience-independent and experience-dependent cues. Animal Behaviour 75, 971–976.Google Scholar
Gwinner, H., Oltrogge, M., Trost, L. and Nienaber, U. (2000). Green plants in starling nests: effects on nestlings. Animal Behaviour 59, 301–309.Google Scholar
Gwinner, H., Yohannes, E., Schwabl, H. (2013). Nest composition and yolk hormones: do female European starlings adjust yolk androgens to nest quality? Avian Biology Research 6, 307–312. http://dx.doi.org/10.3184/175815513X13823680612392 Google Scholar
Heinrich, B. (2013). Why does a Hawk build with green nesting material? Northeastern Naturalist 20, 209–218.Google Scholar
Hurtrez-Boussès, S., Renaud, F., Blondel, J., Perret, P. and Galan, M.-J. (2000). Effects of ectoparasites of young on parents’ behaviour in a Mediterranean population of Blue Tits. Journal of Avian Biology 31, 266–269.Google Scholar
Kim, S.-I., Yi, J.-H., Tak, J.-H. and Ahn, Y.-J. (2004). Acaricidal activity of plant essential oils against Dermanyssus gallinae (Acari: Dermanyssidae). Veterinary Parasitology 120, 297–304.Google Scholar
Kovach, A. G., Szasz, E. (1968). Survival of a pigeon after graded haemorrhage. Acta Physiol Acad Sci Hung 34, 301–309.Google Scholar
Lafuma, L., Lambrechts, M. M. and Raymond, M. (2001). Aromatic plants in bird nests as a protection against blood-sucking flying insects? Behavioural Processes 56, 113–120.CrossRefGoogle ScholarPubMed
Lambrechts, M. M. and Dos Santos, A. (2000). Aromatic herbs in corsican blue tit nests: the “potpourri” hypothesis. Acta Oecologica 21, 175–178.CrossRefGoogle Scholar
Lesna, I., Wolfs, P., Faraji, F., Roy, L., Komdeur, J., and Sabelis, M. W. (2009). Candidate predators for biological control of the poultry red mite dermanyssus gallinae. Experimental and Applied Acarology 48, 63–80.Google Scholar
Loye, J. E. and Zuk, M. (eds.), Clark, L. (contributor). (1991). The nest protection hypothesis: the adaptive use of plant secondary compounds by European starlings. In Bird-Parasite Interactions-Ecology, Evolution and Behaviour. Oxford University Press, Oxford, pp. 204–221.Google Scholar
Malan, G., Parasram, W. A. and Marshall, D. J. (2002). Putative function of green lining in black sparrowhawk nests: mite-repellent role? South African Journal of Science 98, 358–360.Google Scholar
Mennerat, A. (2008). Blue tits Cyanistes caeruleus respond to an experimental change in the aromatic plant odour composition of their nest. Behavioural Processes 79, 189–191.Google Scholar
Mennerat, A., Bonadonna, F., Perret, P. and Lambrechts, M. M. (2005). Olfactory conditioning experiments in a food-searching passerine bird in semi-natural conditions. Behavioural Processes 70, 264–270.CrossRefGoogle Scholar
Mennerat, A., Perret, P., Caro, S. P., Heeb, P. and Lambrechts, M. M. (2008). Aromatic plants in blue tit Cyanistes caeruleus nests: no negative effect on blood-sucking Protocalliphora blow fly larvae. Journal of Avian Biology 39, 127–132.Google Scholar
Mennerat, A., Perret, P. and Lambrechts, M. M. (2009 a). Local individual preferences for nest materials in a passerine bird. Plos ONE 4, e5104.CrossRefGoogle Scholar
Mennerat, A., Mirleau, P., Blondel, J., Perret, P., Lambrechts, M. M. and Heeb, P. (2009 b). Aromatic plants in nests of the blue tit Cyanistes caeruleus protect chicks from bacteria. Oecologia 161, 849–855.Google Scholar
Mennerat, A., Perret, P., Bourgault, P., Blondel, J., Gimenez, O., Thomas, D. W., Lambrechts, M. M. (2009 c). Aromatic plants in nests of blue tits: positive effects on nestlings. Animal Behaviour 77, 569–574.Google Scholar
Milton, S. and Dean, R. (1999). Nesting thyme - the use of aromatic plants in cape sparrow nests. Africa Birds and Birding 1, 37–39.Google Scholar
Mirsky, S. (2008). Shakespeare to blame for introduction of European starlings to US. Scientific American Date accessed: 25/11/14 Available: http://www.scientificamerican.com/article/call-of-the-reviled/ Google Scholar
Ontiveros, D., Caro, J. and Pleguezuelos, J. M. (2008). Green plant material versus ectoparasites in nests of bonelli's eagle. Journal of Zoology 274, 99–104.CrossRefGoogle Scholar
Perrucci, S., Macchioni, G., Cioni, P. L., Flamini, G. and Morelli, I. (1995). Structure/activity relationship of some natural monoterpenes as acaricides against Psoroptes cuniculi . Journal of Natural Products 58, 1261–1264.Google Scholar
Petit, C., Hossaert-McKey, M., Perret, P., Blondel, J. and Lambrechts, M. M. (2002). Blue tits use selected plants and olfaction to maintain an aromatic environment for nestlings. Ecology Letters 5, 585–589.Google Scholar
Pires, B. A., Belo, A. F. and Rabaca, J. E. (2012). Aromatic plants in eurasian blue tit nests: the “nest protection hypothesis” revisited. Wilson Journal of Ornithology 124, 162–165.Google Scholar
Rendell, W. B. and Verbeek, N. A. M. (1996). Old nest material in nestboxes of tree swallows: effects on reproductive success. The Condor 98, 142–152.Google Scholar
Rodgers, J. A. J., Wenner, A. S. and Schwikert, S. T. (1988). The use function of green nest material by wood storks. Wilson Bulletin 100, 411–423.Google Scholar
Sengupta, S. (1981). Adaptive significance of the use of margosa leaves in nests of house sparrows Passer Domesticus . Emu 81, 114–115.Google Scholar
Shutler, D. and Campbell, A. A. (2007). Experimental addition of greenery reduces flea loads in nests of a non-greenery using species, the tree swallow Tachycineta bicolor . Journal of Avian Biology 38, 7–12.Google Scholar
Tomas, G., Merino, S., Martinez-de la Puente, J., Moreno, J., Morales, J., Lobato, E., del Cerro, S. (2012). Interacting effects of aromatic plants and female age on nest-dwelling ectoparasites and blood-sucking flies in avian nests. Behavioural Processes 90, 246–253.Google Scholar
Tripet, F. and Richner, H. (1997). Host responses to ectoparasites: food compensation by parent blue tits. Oikos 78, 557–561.Google Scholar
Tripet, F. and Richner, H. (1999). Dynamics of Hen Flea Ceratophyllus gallinae subpopulations in blue tit nests. Journal of Insect Behavior 12, 159–174.Google Scholar
Veiga, J. and Polo, V. (2012). Female spotless starlings Sturnus unicolor remove green plants from their nests. Journal of Ornithology 153, 291–296.Google Scholar
Wimberger, P. (1984). The use of green plant-material in bird nests to avoid ectoparasites. Auk 101, 615–618.Google Scholar
Wolfs, P. H. J., Lesna, I. K., Sabelis, M. W., Komdeur, J. (2012). Trophic structure of arthropods in starling nests matter to blood parasites and thereby to nestling development. Journal of Ornithology 153, 913–919.Google Scholar
Yang, Y.-C., Lee, S.-H., Lee, W.-J., Choi, D.-H. and Ahn, Y.-J. (2003). Ovicidal and adulticidal effects of Eugenia caryophyllata bud and leaf oil compounds on Pediculus capitis . Journal of Agricultural and Food Chemistry 51, 4884–4888.Google Scholar