Impact of rainfall on the offspring PHA‐response and body mass in the Eurasian blue tit

2018 ◽  
Vol 34 (1) ◽  
pp. 85-93
Author(s):  
Emilia Grzędzicka
Keyword(s):  
Blue Tit ◽  
The Auk ◽  
2003 ◽  
Vol 120 (3) ◽  
pp. 658-668
Author(s):  
Pekka T. Rintamäkt ◽  
Jon R. Stone ◽  
Arne Lundberg

Abstract According to the hypothesis that has been invoked most frequently to explain seasonal fattening patterns for birds—the “adaptive winter-fattening hypothesis”—individuals respond to worsening foraging conditions by increasing body mass and energy reserves. Two hypotheses have been proposed equally frequently to explain daily weight gain patterns for birds: according to the “state-dependent foraging hypothesis,” energy reserves should be amassed early during the day, when starvation risk increases; according to the “mass-dependent predation-risk hypothesis,” mass gain should be delayed for as long as possible, to minimize predation risk. Those hypotheses have been tested previously, using statistical methods (e.g. multiple-regression analysis) that assume independence among environmental variables (e.g. photoperiod and temperature). We conducted path analyses that included four predictor variables (day-in-season, hour-in-day, mean daily temperature, and daily precipitation) to model body-mass fluctuations for two small, nonhoarding (noncaching) passerine species that inhabit central eastern Sweden. Data were partitioned hierarchically into species, age class, gender, and season subgroups. As reported in many small passerine species studies, body mass increased during the day and maximized at dusk; over seasons, body mass increased during autumn, maximized by midwinter, and declined toward breeding in spring. Path analysis models accounted for 9.5–49.9% (mean 26.3%) for Blue Tit (Parus caeruleus) body mass variance and 1.8–52.3% (mean 16.8%) for Great Tit (P. major) body mass variance; for both species, accountability was lowest for autumn (Blue Tit,12.2%; Great Tit, 7.3%), highest for winter (Blue Tit, 33.4%; Great Tit, 21.9%), and intermediate for spring (Blue Tit, 22.7%; Great Tit, 11.8%); for Blue Tits, it was greater for adults than for juveniles (33.2 and 21.7%); whereas negligible for Great Tits (15.9 and 17.3%) and slightly greater for males than for females (Blue Tit, 27.4 and 23.5%; Great Tit, 23.1 and 21.3%). Those results are consistent with predictions formulated on the basis of the adaptive winter-fattening, partially with state-dependent foraging, and, possibly, mass-dependent predation-risk hypothesies and reveal that body-mass fluctuations are associated to a greater extent with photoperiod than with temperature.


2020 ◽  
Vol 31 (3) ◽  
pp. 702-710 ◽  
Author(s):  
Barbara Class ◽  
Jon Brommer

Abstract Repeatable behaviors (i.e., animal personality) are pervasive in the animal kingdom and various mechanisms have been proposed to explain their existence. Genetic and nongenetic mechanisms, which can be equally important, predict correlations between behavior and body mass on different levels (e.g., genetic and environmental) of variation. We investigated multilevel relationships between body mass measured on weeks 1, 2, and 3 and three behavioral responses to handling, measured on week 3, which form a behavioral syndrome in wild blue tit nestlings. Using 7 years of data and quantitative genetic models, we find that all behaviors and body mass on week 3 are heritable (h2 = 0.18–0.23) and genetically correlated, whereas earlier body masses are not heritable. We also find evidence for environmental correlations between body masses and behaviors. Interestingly, these environmental correlations have different signs for early and late body masses. Altogether, these findings indicate genetic integration between body mass and behavior and illustrate the impacts of early environmental factors and environmentally mediated growth trajectory on behaviors expressed later in life. This study, therefore, suggests that the relationship between personality and body mass in developing individuals is due to various underlying mechanisms, which can have opposing effects. Future research on the link between behavior and body mass would benefit from considering these multiple mechanisms simultaneously.


PeerJ ◽  
2017 ◽  
Vol 5 ◽  
pp. e3181 ◽  
Author(s):  
Zhiqiang Zhang ◽  
Chenchen Jin ◽  
Kangshan Qu ◽  
Enrique Caviedes-Vidal

Phytohemagglutinin (PHA)-induced skin swelling response is widely used as a rough surrogate of integrative cell-mediated and innate immunity across multiple vertebrate taxa due to its simplification and feasibility. However, little is known whether there are sex and interspecific differences of immune responsiveness to PHA in ectotherms, especially for anurans. Therefore, we studied sex and species differences of PHA response in three anurans, Asiatic toads (Bufo gargarizans), Dark-spotted frogs (Pelophylax nigromaculatus) and Mongolian toads (Pseudepidalea raddei), captured in northern regions of Anhui Province (China). Footpad thickness was measured prior to (0 h) and after (6, 12, 24, 48 and 72 h) a PHA injection and normalized against saline injection in the opposite footpad. Body mass was recorded at the beginning (0 h) and end of each assay (72 h). Results showed effects of PHA assay, sex and taxa on body mass. Relative maximum swelling response (PHAmax) ranged from 18.58–29.75%, 9.77 to 20.56% and 21.97 to 31.78% and its occurrence over time was apparent 10.6–19.72 h , 7.74–14.01 h and 17.39–23.94 h postinjection for Asiatic toads, Dark-spotted frogs and Mongolian toads, respectively. Finally, the magnitude or timing of PHAmax in Dark-spotted frogs was significantly thinner and faster than in Mongolian toads, and Asiatic toads had an in-between value, not different from the other two species. The magnitude of PHAmax was significantly positively correlated with the timing of PHAmax considering individuals altogether, but not when analyzed within species. Our results indicate that male and female anuran species respond similarly to PHA antigen stimulation, but the magnitude and timing of PHAmax is species-specific. Briefly, we provide new evidence for the suitability of PHA assay in non-model anuran species with different body sizes, and exhort the need to further investigate the nature of PHA assay at the hematological and histological levels in order to extend its application in ecoimmunological studies of amphibians.


2006 ◽  
Vol 273 (1595) ◽  
pp. 1759-1764 ◽  
Author(s):  
Anna Dubiec ◽  
Mariusz Cichoń ◽  
Kinga Deptuch

In birds, poor rearing conditions usually have negative effects on T-cell-mediated immune response. However, earlier studies demonstrate that fitness-related traits such as body mass may show sex-specific patterns when subject to alteration of rearing conditions. Therefore, to investigate whether deterioration of rearing conditions influences the development of immune function differently in male and female nestlings, we performed brood size manipulation experiments on blue tit ( Parus caeruleus ) nestlings. To alter rearing conditions, some broods were increased by three nestlings soon after hatching, while other broods were left non-manipulated. Immune response was assessed as a hypersensitivity reaction to phytohaemagglutinin in 11-day-old nestlings. Additionally, we studied the consequences of brood size manipulation for fledgling body mass and tarsus length. The enlargement of brood size had different effects on the cellular immune responses of male and female nestlings, with males being more negatively affected than their female nest-mates. Sex-specific effects of poor rearing conditions were also recorded for tarsus length, such that tarsus growth was more retarded in female than in male nestlings. We discuss the effects of deterioration of rearing conditions on sex-specific development of cell-mediated immunity with respect to sexual dimorphism of size and developmental strategies in male and female nestlings.


2007 ◽  
Vol 177 (4S) ◽  
pp. 64-64
Author(s):  
Murugesan Manoharan ◽  
Martha A. Reyes ◽  
Alan M. Nieder ◽  
Bruce R. Kava ◽  
MarkS Soloway

2006 ◽  
Vol 175 (4S) ◽  
pp. 155-155
Author(s):  
Robert L. Grubb ◽  
David L. Levin ◽  
Paul F. Pinsky ◽  
Jerome Mabie ◽  
Thomas L. Riley ◽  
...  

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