Back to index of mangrove and seagrass research projects

Back to index of 2002 research reports

SIGNALLING BEHAVIOUR IN THE FIDDLER CRAB, UCA VOCANS

Introduction

Fiddler crabs inhabit intertidal sand and mud flats, living in dense colonies. The male fiddler crabs have one massively enlarged claw, which is used in fighting with other males and for signalling to females. Pope (1999) investigated claw waving in male fiddler crabs in response to both rival male signals and receptive females. In agreement with an original study by Salmon and Stout (1962), Pope found that males waved significantly more in the presence of females regardless of whether other males were present. Hyatt and Salmon (1997) investigated the behavioural response of male combat in fiddler crabs, furthering work (Crane 1966, 1975) that identified 21 combat acts. Studies by Hazlett (1968) and Schein (1975) indicate that a combatent who is larger has an advantage in winning fights. Research by Land has shown that larger rivals are perceived as a threat by male crabs which will retreat into their burrows, whereas similar or smaller crabs evoke normal competitive claw waving behaviour.

 

Aims

This study aims to examine a range of possible features of waving claws that may influence the responses of target males in their waving behaviour. This will be achieved by manipulating the appearance of a model claw in the following ways:

1.       Size of model claw- slow, medium and large

2.       Speed of waving model claw- slow, medium and fast

3.       Distance of model claw to the subject – (e.g. 2cm, 1cm, 0cm). This will be manipulated to allow a match in the apparent size of different sized model claws at different distances (e.g. using a medium sized claw at a close distance to appear the same size as a large claw at a greater distance). This will assess whether the crabs use this simple rule to judge the apparent threat of a rival as a simple combination of size and distance. 

 

Method

A sample of fiddler crab claws will be assessed to establish the natural range in claw sizes in the population. The extreme values in this data will be used to determine the two marginal manipulation values, with the third one being equidistant between the two. Model claws will be taken from dead crabs or those found released by autotomy. A container will be made out of wood to prevent any reflections that would occur from using a glass tank. A sample crab will be place in the middle of the container with enough room to escape backwards and about 1m of space infront for the model to be manipulated. Once the sample crab has acclimatised to its new surrounding its response will be recorded when stimulated by the models. The model claws will be glued onto a stick and pushed to a measured distance in front of the crab where waving response will be recorded.  Each male crab will be marked with a number on its carapace allowing the results to be repeated. Each of the 27 possible treatment combinations will be presented to each subject in a randomised order with sufficient time before hand to allow the crab to acclimatise.

 

Preliminary results

Crabs respond more aggressively to a similar or smaller sized claw at a closer distance.  If the crab is stimulated with a larger claw then it will retreat unless the claw is at 0cm when the crab must attack as a last resort. None of the crabs showed any habituation to the stimulus. 

The percentage waving responses of a target male crab to each experimental treatment will be analysed in a within-subjects design. The effects of the model claw size, distance and waving frequency will be analysed using a three-way repeated measure ANOVA, or in a number of smaller models if all possible treatment combinations are unavailable for too many subjects. Additional variables could be used to explain additional amounts of the variation in responses within these models.

 

Report

A final year dissertation report will be completed by Paul Rollinson, University of Bangor by May 2003.