Weapon size is a reliable indicator of strength and social dominance in female slender crayfish (Cherax dispar)

Weapons are specialized structures that are commonly used by animals to signal fighting ability and resource holding potential during agonistic encounters. Current theory predicts weapon size should reliably indicate weapon strength and unreliable signals should only occur at very low frequencies in nature. However, a recent study found weapon size was an unreliable signal of strength during agonistic interactions among males of the slender crayfish (Cherax dispar). In this study, we investigated the relationship between morphology, performance and social dominance in females of C. dispar. Based on current theory, we predicted chela size would reliably indicate chela strength and would relate indirectly to dominance via its influence on strength. We found females that possessed large chelae were more likely to possess stronger chelae, and those individuals with stronger chelae were more likely to win competitive bouts. The best predictive model of the relationships among morphology, performance and dominance indicated chela size indirectly affected social dominance via its influence on strength, thus demonstrating displays of weaponry are reliable signals of fighting ability. Reliable signals of strength among females of C. dispar supports current theory predicting stable signalling systems should largely consist of honest displays of strength. However, this contrasts with previous work demonstrating that male C. dispar routinely uses unreliable signals of weapon strength during agonistic encounters

Lizards paid a greater opportunity cost to thermoregulate in a less heterogeneous environment

1. The theory of thermoregulation has developed slowly, hampering efforts to predict how individuals can buffer climate change through behaviour. Mixed results of field and laboratory experiments underscore the need to test hypotheses about thermoregulation explicitly, while measuring costs and benefits in different thermal landscapes. 2. We simulated body temperature and energy expenditure of a virtual lizard that either thermoregulates optimally or thermoconforms in a landscape of either low or high quality (one or four basking sites, respectively). We then compare the predicted values in each landscape with the observed values for real lizards in experimental arenas. 3. Lizards thermoregulated more accurately in the high-quality landscape than they did on the low-quality landscape, albeit only slightly so, but spent similar amounts of energy in these landscapes. Basking, rather than shuttling between heat sources, accounted for the majority of the energy consumed in both landscapes. 4. These results did not support the predictions of our model. In the low-quality landscape, real lizards thermoregulated intensely despite the potential to save energy by thermoconforming. In the high-quality landscape, lizards moved more than expected, suggesting that lizards explored their surroundings despite being able to thermoregulate without doing so. 5. Our results suggest that non-energetic benefits drive thermoregulatory behaviour in costly environments, despite the missed opportunities arising from thermoregulation. We propose that energetic costs associated with thermoregulatory movement will become substantial in homogeneous environments such as flat plains and dense forests. The theory of thermoregulation should incorporate these aspects if biologists wish to predict responses of ectotherms to changing climates and habitats

Estimating the adaptive potential of critical thermal limits: Methodological problems and evolutionary implications

1.Current studies indicate that estimates of thermal tolerance limits in ectotherms depend on the experimental protocol used, with slower and presumably more ecologically relevant rates of warming negatively affecting the upper thermal limits (CTmax). Recent empirical evidence also gives credence to earlier speculations suggesting that estimates of heritability could drop with slower heating rates. 2.Using published data from the fruit fly Drosophila melanogaster, we show that empirical patterns can be explained if flies' physical condition decreases with experimental time in thermal tolerance assays. This problem could even overshadow potential benefits of thermal acclimation, also suggesting that a drop in CTmax with slower heating rates does not necessarily rule out beneficial acclimatory responses. 3.Numerical results from a simple illustrative model show that no clear conclusions can be obtained on how the phenotypic variance in CTmax will be affected with different rates of thermal change. Conversely, the genetic variance and estimated heritabilities are expected to drop with slower heating rates, hence ramping rates in experiments aiming to study the evolutionary potential of thermal tolerance to respond to global warming should be as fast as possible (within the range in which measurement accuracy and physical condition are not affected). 4.Measurements under ecologically realistic warming rates should also consider the impact of other physiological and behavioural strategies that might partly compensate the negative effects of slow heating rates. However, there are situations in which slow heating rates closely mimic natural conditions, as those encountered by some aquatic ectotherms. These heating rates may be an issue of major concern in these species, given its negative impact on CTmax and its adaptive potential. © 2010 The Authors. Functional Ecology © 2010 British Ecological Society.Peer Reviewe

The fast and the fractalous: speed and tortuosity trade off in running ants

The thermal sensitivity of locomotor performance has often been described in terms of speed, but the trajectory of locomotion may play an equally important role in capturing prey or escaping predators. Hypotheses based on physical constraints or behavioural plasticity predict relationships between the speed and the tortuosity of running, which should affect the thermal sensitivity of locomotion. We measured the speed and tortuosity of running by leaf-cutter ants over a range of temperatures from 10 °C to 40 °C. Tortuosity was estimated by the fractal dimension of each path. As we expected, ants ran faster at higher temperatures, but they also followed straighter (less tortuous) paths. A negative relationship between speed and tortuosity was observed both within and among thermal environments. Both biomechanical and behavioural mechanisms might have caused the observed relationship. Turning at high speeds should be more difficult because of the force needed to overcome inertia, and turning at low speeds could help ants evade a predator. Staged encounters with predators should help to define the ecological significance of the trade-off between speed and tortuosity