» Articles » PMID: 19633988

Aromatic Plants in Nests of the Blue Tit Cyanistes Caeruleus Protect Chicks from Bacteria

Overview
Journal Oecologia
Date 2009 Jul 28
PMID 19633988
Citations 33
Authors
Affiliations
Soon will be listed here.
Abstract

Several bird species add fresh fragments of plants which are rich in volatile secondary compounds to their nests. It has been suggested, although never tested, that birds use fresh plants to limit the growth of nest microorganisms. On Corsica, blue tits (Cyanistes caeruleus) incorporate fresh fragments of aromatic plants into their nests. These plants do not reduce infestation by nest ectoparasites, but have been shown to improve growth and condition of chicks at fledging. To understand the mechanisms underlying such benefits, we experimentally tested the effects of these plants on the bacteria living on blue tits. Aromatic plants significantly affected the structure of bacterial communities, in particular reducing bacterial richness on nestlings. In addition, in this population where there is a strong association between bacterial density and infestation by blood-sucking Protocalliphora blow fly larvae, these plants reduced bacterial density on the most infested chicks. Aromatic plants had no significant effect on the bacteria living on adult blue tits. This study provides the first evidence that fresh plants brought to the nests by adult birds limit bacterial richness and density on their chicks.

Citing Articles

Effects of experimental nest treatment with herbs on ectoparasites and body condition of nestlings.

Gladalski M, Norte A, Bartos M, Demesko I, Kalinski A, Markowski M Behav Ecol. 2024; 36(1):arae103.

PMID: 39734641 PMC: 11680675. DOI: 10.1093/beheco/arae103.


Nest secondary plants and their associations with haemosporidian blood parasites in blue tit females.

Garcia-Campa J, Gonzalez-Braojos S, Morales J Parasitology. 2024; 151(10):1126-1136.

PMID: 39530248 PMC: 11894026. DOI: 10.1017/S0031182024000775.


Microbiota and the volatile profile of avian nests are associated with each other and with the intensity of parasitism.

Mazorra-Alonso M, Peralta-Sanchez J, Heeb P, Jacob S, Martin-Vivaldi M, Martinez-Bueno M FEMS Microbiol Ecol. 2024; 100(10).

PMID: 39049462 PMC: 11407443. DOI: 10.1093/femsec/fiae106.


Environmental conditions influence host-parasite interactions and host fitness in a migratory passerine.

Gonzalez-Bernardo E, Moreno-Rueda G, Camacho C, Martinez-Padilla J, Potti J, Canal D Integr Zool. 2024; 20(2):256-273.

PMID: 38978458 PMC: 11897943. DOI: 10.1111/1749-4877.12864.


Does nest occupancy by birds influence the microbial composition?.

Xin J, Cao H, Bao X, Hu C Front Microbiol. 2023; 14:1232208.

PMID: 38053547 PMC: 10694247. DOI: 10.3389/fmicb.2023.1232208.


References
1.
Soler J, de Neve L, Perez-Contreras T, Soler M, Sorci G . Trade-off between immunocompetence and growth in magpies: an experimental study. Proc Biol Sci. 2003; 270(1512):241-8. PMC: 1691245. DOI: 10.1098/rspb.2002.2217. View

2.
Mennerat A, Perret P, Lambrechts M . Local individual preferences for nest materials in a passerine bird. PLoS One. 2009; 4(4):e5104. PMC: 2659446. DOI: 10.1371/journal.pone.0005104. View

3.
Sherman P, Hash G . Why vegetable recipes are not very spicy. Evol Hum Behav. 2001; 22(3):147-163. DOI: 10.1016/s1090-5138(00)00068-4. View

4.
Tschirren B, Richner H . Parasites shape the optimal investment in immunity. Proc Biol Sci. 2006; 273(1595):1773-7. PMC: 1634790. DOI: 10.1098/rspb.2006.3524. View

5.
Fauth P, Krementz D, Hines J . Ectoparasitism and the role of green nesting material in the European starling. Oecologia. 2017; 88(1):22-29. DOI: 10.1007/BF00328399. View