scholarly journals Geographic Variation in the Status Signals of Polistes dominulus Paper Wasps

PLoS ONE ◽  
2011 ◽  
Vol 6 (12) ◽  
pp. e28173 ◽  
Author(s):  
Elizabeth A. Tibbetts ◽  
Oksana Skaldina ◽  
Vera Zhao ◽  
Amy L. Toth ◽  
Maksim Skaldin ◽  
...  
Toxicon ◽  
2006 ◽  
Vol 48 (4) ◽  
pp. 473-475 ◽  
Author(s):  
Claudia Bruschini ◽  
Francesca R. Dani ◽  
Giuseppe Pieraccini ◽  
Francesco Guarna ◽  
Stefano Turillazzi

1997 ◽  
Vol 45 (2) ◽  
pp. 95 ◽  
Author(s):  
J. D. Roberts

I analysed geographic variation in advertisement call of tetraploid forms of Neobatrachus. Comparing five regional samples spanning the range of N. kunapalari, there was significant geographic variation in pulses per call but not in dominant frequency, pulse rate, pulse duration or percentage rise time. The call of N. kunapalari was significantly different from four other samples covering the geographic range of tetraploid forms across Australia in all but percentage rise time. Calls of frogs from Mt Magnet in Western Australia (WA) differed from calls from Port Hedland (WA) in pulse duration and in multivariate descriptions but were similar in pulse rate. Pulse rates of calls from N. centralis on Eyre Peninsula in South Australia (SA) were distinct from all other populations sampled but in multivariate space these calls were similar to calls of N. sudellifrom eastern Australia. There may be an eastwest cline in call from N. sudelli to calls of N. aquilonius and N. centralis in WA. Call data support the recognition of two tetraploid species: N. kunapalari and N. sudelli. N. sudelli exhibits geographic variation in call, but the status of N. aquilonius and N. centralis as possible synonyms of N. sudelli was not resolved.


2018 ◽  
Vol 10 (5) ◽  
pp. 690-696 ◽  
Author(s):  
Stephen M. Garcia ◽  
Kimberlee Weaver ◽  
Patricia Chen
Keyword(s):  

1985 ◽  
Vol 19 (2) ◽  
pp. 238 ◽  
Author(s):  
Jeffrey E. Lovich ◽  
Carl H. Ernst ◽  
Steve W. Gotte

2008 ◽  
Vol 4 (3) ◽  
pp. 237-239 ◽  
Author(s):  
Elizabeth A Tibbetts ◽  
Rebecca Lindsay

Aggressive competition is an important aspect of social interactions, but conflict can be costly. Some animals are thought to minimize the costs of conflict by using conventional signals of agonistic ability (i.e. badges of status) to assess rivals. Although putative badges have been found in a range of taxa, little research has tested whether individuals use badges to assess potential rivals before they engage in aggressive contests. Here, choice trials were used to test how the variable black facial patterns in Polistes dominulus wasps are used during rival assessment. Focal wasps were given access to two patches of food, each guarded by a wasp whose facial pattern had been experimentally altered. Wasps chose food patches based on the facial pattern of the guard, preferring to challenge guards with facial patterns indicating a low level of quality, while avoiding guards with facial patterns indicating a high level of quality. Therefore, status badges play an important role during rival assessment; paper wasps use facial patterns alone to quickly assess the agonistic abilities of strangers.


2016 ◽  
Vol 113 (30) ◽  
pp. 8478-8483 ◽  
Author(s):  
Elizabeth A. Tibbetts ◽  
Katherine Crocker ◽  
Zachary Y. Huang

Decades of behavioral endocrinology research have shown that hormones and behavior have a bidirectional relationship; hormones both influence and respond to social behavior. In contrast, hormones are often thought to have a unidirectional relationship with ornaments. Hormones influence ornament development, but little empirical work has tested how ornaments influence hormones throughout life. Here, we experimentally alter a visual signal of fighting ability in Polistes dominulus paper wasps and measure the behavioral and hormonal consequences of signal alteration in signalers and receivers. We find wasps that signal inaccurately high fighting ability receive more aggression than controls and receiving aggression reduces juvenile hormone (JH) titers. As a result, immediately after contests, inaccurate signalers have lower JH titers than controls. Ornaments also directly influence rival JH titers. Three hours after contests, wasps who interacted with rivals signaling high fighting ability have higher JH titers than wasps who interacted with rivals signaling low fighting ability. Therefore, ornaments influence hormone titers of both signalers and receivers. We demonstrate that relationships between hormones and ornaments are flexible and bidirectional rather than static and unidirectional. Dynamic relationships among ornaments, behavior, and physiology may be an important, but overlooked factor in the evolution of honest communication.


2020 ◽  
Vol 74 (11) ◽  
Author(s):  
Mirjam J. Borger ◽  
Lauren E. Johnson ◽  
Nathaly O. Salazar ◽  
Cameron L. Dreghorn ◽  
Jan Komdeur ◽  
...  

Abstract Status signals have evolved for individuals to avoid energetic and physical costs of resource defense. These signals reflect an individual’s competitive ability and therefore influence competitors’ decisions on how to invest in a fight. We hypothesized that the response of receivers to status signals will depend on the social context. During territorial defense, group members may provide support to a territory owner by participating in defense. We investigated whether the presence of juveniles—who group together with territorial males—alters the territorial male’s attack decisions and level of aggression in the black-crested titmouse (Baeolophus atricristatus). Crest-length in this species functions as status signal. We simultaneously presented two taxidermic male models in a territory: one with an unmanipulated crest and one with a modified shortened crest. Models were presented to males that had resident juveniles cohabiting on their territory, and to males without juveniles. During intrusions, juveniles actively defended against the simulated intruders by approaching and sometimes attacking. The presence of juveniles affected how territorial males responded to the status signals of the intruders: when juveniles were present, males were more likely to first attack the model with the unmanipulated crest (i.e., longer, and more threatening), compared to males residing without juveniles. This suggests that juvenile support alters the risk-taking decision of the territorial male. To our knowledge, this is the first indication that behavioral responses to a status signal depends on the presence of supportive group members. Significance statement Status signals can indicate relative quality of animals and can therefore be used to evaluate a competitor when deciding whether or not to fight over resources. The black-crested titmouse has been shown to use its crest length as a status signal during fights over food. In our study, we assessed if this status signal is also used in territorial defense, by conducting an experiment where we presented two taxidermic male models with different crest sizes to a territorial male. We also investigated whether juvenile presence influenced which model was attacked. In trials where juveniles were present, territorial males attacked the longer crested model significantly more often than in trials where territorial males were alone. This suggests that the presence of juveniles, which help the male defend the territory, allows the male to attack the more aggressive-appearing intruder.


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