scholarly journals Geographic variation in call structure, likelihood, and call-song associations across subspecies boundaries, migratory patterns, and habitat types in the Marsh Wren (Cistothorus palustris)

The Auk ◽  
2018 ◽  
Vol 135 (1) ◽  
pp. 127-151 ◽  
Author(s):  
Sarah A. M. Luttrell ◽  
Bernard Lohr
The Condor ◽  
2007 ◽  
Vol 109 (2) ◽  
pp. 389-398 ◽  
Author(s):  
Susannah C. Buhrman-Deever ◽  
Amy R. Rappaport ◽  
Jack W. Bradbury

Abstract Introduced feral populations offer a unique opportunity to study the effects of social interaction and founder effects on the development of geographic variation in learned vocalizations. Introduced populations of Monk Parakeets (Myiopsitta monachus) have been growing in number since the 1970s, with a mixture of isolated and potentially interacting populations. We surveyed diversity in contact calls of Monk Parakeet populations in Connecticut, Texas, Florida, and Louisiana. Contact call structure differed significantly among the isolated populations in each state. Contact call structure also differed significantly among potentially interacting nest colonies in coastal Connecticut, and these differences did not follow a geographic gradient. Limited dispersal distances, founder effects, and social learning preferences may play a role in call structure differences.


Copeia ◽  
2003 ◽  
Vol 2003 (4) ◽  
pp. 750-758 ◽  
Author(s):  
Michael J. Smith ◽  
William Osborne ◽  
David Hunter

Author(s):  
Peter Berthold

The study of migratory behavior is, at a fundamental level, the study of geographic variation in behavior. This is necessarily the case when residency grounds at either end of the migratory route differ in spatial extent, because different directional movement patterns will be required of individuals from different parts of the two ranges. As many migratory animals are widespread, substantial differences in migratory routes exist among populations of single species (examples in Dadswell et al. 1987, Baker 1991, Dingle 1991, Groot and Margolis 1991, Berthold 1993). Because the individuals that migrate often have not done so before and often do not have older migration-experienced individuals to follow (e.g., Baker 1991, Berthold 1996), the study of navigational mechanisms and their genetic underpinnings is essential to understanding migratory behavior. Naturalists have long been captivated by the problem of control mechanisms in migratory behavior. As early as 1702, von Pernau suggested that birds were “driven at the proper time by a hidden drive.” In modern terms, this amounted to suggesting that migratory behavior was triggered by innate or genetically programmed stimuli, rather than by environmental factors alone. This speculation was supported by the discovery of endogenous annual cycles more than 260 years later (see Gwinner 1986 for a review). Our understanding of the control mechanisms of migratory behavior has expanded rapidly during the last 90 years. Research in the field has elucidated, for example, genetic and endocrine control mechanisms and their interface with environmental cues such as photoperiod, relationships between environmental conditions, such as weather and food availability and the timing of migration, and unique physiological and morphological correlates of migratory behavior (for reviews, see Berthold and Terrill 1991, Berthold 1996). Birds, fishes, and insects have proven especially valuable subjects for the study of migratory behavior, and all show substantial population differentiation in migratory patterns within species (Dadswell et al. 1987, Dingle 1991, Groot and Margolis 1991, Berthold 1993). In this chapter I focus on migratory behavior in birds, especially that in the blackcap, Sylvia atricapilla, an Old World warbler that has been the subject of extensive research in my laboratory since the early 1970s.


2019 ◽  
Author(s):  
Marko J. Spasojevic ◽  
Sören Weber1

Stable carbon (C) and nitrogen (N) isotopes in plants are important indicators of plant water use efficiency and N acquisition strategies. While often regarded as being under environmental control, there is growing evidence that evolutionary history may also shape variation in stable isotope ratios (δ13C and δ15N) among plant species. Here we examined patterns of foliar δ13C and δ15N in alpine tundra for 59 species in 20 plant families. To assess the importance of environmental controls and evolutionary history, we examined if average δ13C and δ15N predictably differed among habitat types, if individual species exhibited intraspecific trait variation (ITV) in δ13C and δ15N, and if there were a significant phylogenetic signal in δ13C and δ15N. We found that variation among habitat types in both δ13C and δ15N mirrored well-known patterns of water and nitrogen limitation. Conversely, we also found that 40% of species exhibited no ITV in δ13C and 35% of species exhibited no ITV in δ15N, suggesting that some species are under stronger evolutionary control. However, we only found a modest signal of phylogenetic conservatism in δ13C and no phylogenetic signal in δ15N suggesting that shared ancestry is a weaker driver of tundra wide variation in stable isotopes. Together, our results suggest that both evolutionary history and local environmental conditions play a role in determining variation in δ13C and δ15N and that considering both factors can help with interpreting isotope patterns in nature and with predicting which species may be able to respond to rapidly changing environmental conditions.


2008 ◽  
Vol 34 (3) ◽  
pp. 288-302 ◽  
Author(s):  
Julie N. Oswald ◽  
Shannon Rankin ◽  
Jay Barlow
Keyword(s):  

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