Individual and status recognition in the crayfish, Orconectes rusticus: the effects of urine release on fight dynamics

Summary This study examined individual and status recognition in dyadic interactionsbetween cray sh and determines how blocking the release of urine, a known source of chemical cues, may in uence recognition. Behavioral characteristics of agonistic interactions were compared between cray sh pairs that fought each other previously (familiar) and pairs derived from individuals with past status history but no previous experience with one another (unfamiliar). To address the role of urine born chemical cues in recognition, ght dynamics were examined in urine blocked and non-blocked familiar and unfamiliar pairs. Our results indicate the existence of status recognitionin cray sh as rst ghts were longer than second ghts and the statistical interaction between ght number and familiar/unfamiliar treatment was similar. Urine cues play a role in social recognition in that ghts are longer and more intense when urine cues are absent than when urine cues are present. Communication of behavioral state through urine appears to play an important role in the agonistic interactions of cray sh

Behavioral differences in an over‐invasion scenario: marbled vs. spiny‐cheek crayfish

New species often invade ecosystems already dominated by previous invaders. Ornamental freshwater crayfish, particularly parthenogenetic marbled crayfish (Procambarus virginalis), increasingly establish in European water bodies where they interact with resident native and non‐native species. Behavioral traits and behavioral syndromes can influence the outcome of these species interactions. The behavior of non‐native crayfish is often studied in notorious invaders but rarely in new and emerging species, although those provide the best opportunity for management. Activity, aggressiveness, and boldness have repeatedly been associated with invasion success and species displacement. Further, crayfish can adapt their behavior after they have established in the new range. We investigated whether marbled crayfish can displace the widely established spiny‐cheek crayfish (Orconectes limosus). Specifically, we compared their behavioral traits and evaluated whether these traits differ, using marbled crayfish populations from aquaria and the field and spiny‐cheek crayfish from the field. We staged agonistic encounters, measured activity levels, and recorded the response to a simulated threat of both species and both origins (field and aquarium) in laboratory trials. We found that in agonistic encounters, marbled crayfish were on average more aggressive than spiny‐cheek crayfish, even against larger opponents. Aggressiveness and activity were positively correlated, which is indicative for an aggression syndrome. Marbled crayfish from the field were less active than those from aquaria, but there was no difference in aggressiveness. Marbled crayfish often froze in response to a simulated threat, whereas spiny‐cheek crayfish reacted either offensively or defensively. These results from the laboratory illustrate potentially important behavioral mechanisms behind crayfish over‐invasions and show behavioral plasticity in a species where all known individuals are genetically identical. To better understand the invasion process in nature, the species’ reproductive biology and interactions with other members of the community should be considered. We conclude that the recent success of marbled crayfish in establishing new populations could be influenced by their behavioral flexibility and their potential to competitively persist in the presence of established invasive crayfish

Crayfish Recognize the Faces of Fight Opponents

The capacity to associate stimuli underlies many cognitive abilities, including recognition, in humans and other animals. Vertebrates process different categories of information separately and then reassemble the distilled information for unique identification, storage and recall. Invertebrates have fewer neural networks and fewer neural processing options so study of their behavior may reveal underlying mechanisms still not fully understood for any animal. Some invertebrates form complex social colonies and are capable of visual memory–bees and wasps, for example. This ability would not be predicted in species that interact in random pairs without strong social cohesion; for example, crayfish. They have chemical memory but the extent to which they remember visual features is unknown. Here we demonstrate that the crayfish Cherax destructor is capable of visual recognition of individuals. The simplicity of their interactions allowed us to examine the behavior and some characteristics of the visual features involved. We showed that facial features are learned during face-to-face fights, that highly variable cues are used, that the type of variability is important, and that the learning is context-dependent. We also tested whether it is possible to engineer false identifications and for animals to distinguish between twin opponents

Data from: A novel alarm signal in aquatic prey: Familiar minnows coordinate group defences against predators through chemical disturbance cues

Animal signalling systems outside the realm of human perception remain largely understudied. These systems consist of four main components: a signalling context, a voluntary signal, receiver responses and resulting fitness benefits to both the signaller and receiver(s). It is often most difficult to determine incidental cues from voluntary signals. One example is chemical disturbance cues released by aquatic prey during predator encounters that may serve to alert conspecifics of nearby risk and initiate tighter shoaling. We aimed to test whether disturbance cues are released incidentally (i.e. as a cue) or are produced voluntarily depending on a specific signalling context such as the audience surrounding the individual, and thus constitute a signal. We hypothesized that if receivers use disturbance cues to communicate risk among themselves, they would produce more (or more potent) disturbance cues when present in a group of conspecifics rather than when they are isolated (presence/absence of an audience) and use disturbance cues more when present alongside familiar rather than unfamiliar conspecifics (audience composition effect). We placed fathead minnows (Pimephales promelas) in groups with familiar fish, unfamiliar fish or as isolated individuals with no audience present, and then simulated a predator chase to evoke disturbance cues. We used bioassays with independent receivers to assess whether the disturbance cues produced differed depending on the signallers’ audience. We found evidence of voluntary signalling, as minnows responded to disturbance cues from groups of fish with tighter shoaling while disturbance cues from isolated minnows did not evoke a significant shoaling response (presence/absence audience effect). Receivers also increased shoaling, freezing and dashing more in response to disturbance cues from familiar groups compared to disturbance cues from unfamiliar groups or isolated minnows (audience composition effect). Together, these findings support our hypothesis that disturbance cues are used as an antipredator signal to initiate coordinated group defences among familiar conspecifics involving shoaling, freezing and dashing. This study represents the strongest evidence to date that chemicals released by aquatic prey upon disturbance by predators serve as voluntary signals rather than simply cues that prey have evolved to detect when assessing their risk of predation