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First published online January 19, 2006
Journal of Experimental Biology 209, 393-398 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02000
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Textbook cricket goes to the field: the ecological scene of the neuroethological play

Olivier Dangles, Jérôme Casas* and Isabelle Coolen

Université de Tours, IRBI UMR CNRS 6035, Parc Grandmont, 37200 Tours, France


Figure 1
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Fig. 1. Experimental design used to assess the importance of natural predators on cricket behaviour and survival. For each treatment, cages were built so as to allow for a single type of predation. (A) Cages for the `air' treatment had an open top to allow flying predators to access the encaged crickets, and a plastic border at the top of the cages on which fluon was applied to prevent escapes or unwanted intrusions. (B,C) Cages for the `spider' (B) and the `control' (C) treatments were closed at the top with mosquito screen. All cages had a wooden frame of 0.5 mx0.5 mx0.25 m covered with clear plastic on the sides and a fabric bottom. In total, we used 225 juvenile crickets of stage 2-3, 225 juvenile crickets of stage 4-5 and 90 adults (45 males and 45 females), all caught from the local population. Behavioural and survival data were collected once a week from each cage. The experimenter first watched the inside of the cages from above for 1 min and counted the number of crickets from each age category that were visible at the surface of leaves, and then made an exhaustive count of the number of crickets still alive. The computed proportion of individuals visible at the surface of leaves was compared among treatments using ANOVA. To ensure that the effect seen on the proportions was not a byproduct of the total number of individuals still alive, proportions were weighted by numbers still alive before being compared among treatments. Given that total numbers still alive were not found to differ significantly among cages, the weight used was the mean number still alive for each cage over weeks. Survival data were directly obtained through the exhaustive count of crickets. Survival data were compared among treatments independently for juveniles of stage 2-3, juveniles of stage 4-5, and adults, using Tarone-Ware survival tests.

 

Figure 2
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Fig. 2. Cricket survival and hiding behaviour as a function of predator type. Proportion of (A) juveniles of stage 2-3, (B) juveniles of stage 4-5 and (C) adult crickets still alive on a given week after initiation of treatments. The `control', `air' and `spider' treatments are represented by the full, broken and dotted line, respectively. Survival was compared among treatments independently for juveniles of stage 2-3, juveniles of stage 4-5 and adults using Tarone-Ware survival tests. (D) Proportion of juveniles of stage 2-3, juveniles of stage 4-5 and adult crickets seen at the surface of leaves during 1 min of observation in the three different treatments. The proportion of individuals visible at the surface of leaves was compared among treatments using ANOVA. Values are means ± s.e.m.

 

Figure 3
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Fig. 3. Framework to study the ecological significance of crickets' escape system. (1) The identity of the predator greatly affects the nature of the stimulus perceived by the cricket. (2) The relative conspicuousness of a stimulus can be strongly affected by how well it transmits through the local environment. Although undocumented in crickets, signal perception has been related to habitat type in bats and fishes (Jones and Rydell, 1994Go; Domenici and Blake, 1997Go). Background noise (e.g. wind) may also impair crickets' ability to extract information from stimuli. (3) Hunting tactics of crickets' predators are likely to be influenced by the surrounding environment as shown for other predators. Bats for example, increase both the frequency and the bandwidth of their echo during target approach, thereby reducing the masking effect produced by the cluttering of nearby vegetation (Jones and Rydell, 1994Go). (4) Behaviour and therefore survival of crickets vary depending on the identity of predators (this study) and their attack tactic (Dangles et al., 2006Go). In return, cricket behaviour is likely to influence predator tactics. (5) Cricket cercus morphology is variable among populations from different environments (Dangles et al., 2005Go), suggesting an influence of predator and/or environmental characteristics on cercus morphology. Such a reaction norm is well documented in aquatic organisms that are capable of inducing defences (e.g. spines) in the presence of predators (see Schlichting and Pigliucci, 1998Go).

 

Figure 4
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Fig. 4. Illustration of cricket-predator interactions in two contrasting habitats: (A) Temperate forest ground (France). The predation by wolf spiders (Pardosa sp.) on wood crickets (Nemobius sylvestris) takes place in the complex three-dimensional structure of the ground litter. The air flow produced by the spider is linear, coming from one direction. (B) Tropical cave wall (Gabon). Cave crickets (e.g. Phalangopsidae) are commonly preyed upon by whip spiders (Amblypygi sp.) in various tropical regions around the world (O.D., unpublished; Louis Deharveng, National Natural History Museum of Paris, personal communication). In contrast to A, this interaction occurs on a simple structure, the bare and flat walls of caves. The air flow produced by the two raptorial pedipalps of the whip spider comes from opposite directions. Cave pictures by Richard Oslisly/WCS Gabon.

 





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