Grooming behaviors reduce fouling of body regions. In decapods, grooming time budgets, body regions groomed, and grooming appendages are known in several species; however, little data exists on brachyuran crabs. In this study, grooming behaviors of two commercially important crabs were documented (blue crabs: Callinectes sapidus Rathbun, 1896; stone crabs: Menippe mercenaria Say, 1818). These crabs are harvested by fishermen and knowing their grooming behaviors is valuable, as clean crabs are preferred by consumers and the stone crab fishery consequence of removing one cheliped to grooming behaviors is unknown. Crabs were observed individually and agonistically to determine how grooming behaviors vary in the presence of another conspecific. Both species frequently use their maxillipeds and groom, with the gills being cleaned by epipods. Respiratory and sensory structures were groomed frequently in both species. Removal of a grooming appendage resulted in higher fouling levels in the gills, indicating that grooming behaviors do remove fouling. Overall, stone crabs had a larger individual time budget for grooming, but agonistic grooming time budgets were similar. Stone crab chelipeds are used in grooming, especially cleaning the other cheliped. The chelipeds are not the main grooming appendage; however, implications of losing one cheliped may have large impacts.
In crustaceans, grooming behaviors decrease fouling by removing debris from the exoskeleton and body structures; these grooming behaviors improve respiration, sensory reception, movement, and reproduction. Setal morphologies of the following grooming appendages in the decapod crustacean spider crab Libinia dubia are examined including the first pereiopod (cheliped), first, second, and third maxillipeds (mouthparts), and first, second, and third epipods (internal extensions of the maxillipeds). The objective of this study was to describe setal morphologies of these grooming appendages and to elucidate possible functions and efficiencies of setal structures. Spider crabs are hypothesized to have elaborate setal morphologies, mainly for cleaning specialized decorating setae as well as for cleaning inside the gill chamber, which has a higher likelihood of becoming fouled compared to other decapods such as shrimps. Fourteen setal types are documented and included several varieties of serrate and pappose setae as well as simple setae, cuspidate setae, papposerrate setae, and canoe setae. Maxillipodal epipods in the gill chamber are free of fouling, suggesting the setation on the third maxilliped protopod has an efficient functional morphology in removing debris before water enters the gill chamber. Serrate setae may function for detangling and separating structures whereas pappose setae may function for fine detailed grooming. The cheliped is the only grooming appendage that can reach decorating setae and it contains only pappose setae; thus decorating setae is not likely groomed in a manner that would greatly decrease fouling. J. Morphol. 277:1045-1061, 2016. © 2016 Wiley Periodicals, Inc.
Body fouling has been reduced by grooming behaviors. In decapods, grooming has been focused on gills, sensory structures, and jointed appendages. In this study, grooming behaviors of the spider crab, Libinia dubia H. Milne-Edwards, 1834, were examined; this brachyuran crab decorates and camouflages body regions by attaching materials onto hooked setae. The relationship between grooming and these camouflaged body regions was unknown. Six observational and experimental studies examined the grooming frequency, duration of grooming behaviors, body regions groomed, variance of these behaviors in the presence of another individual, and the efficiency of these grooming behaviors at removing gill fouling. Sensory and respiratory structures were groomed most frequently and for the longest duration, not body regions with decorations and hooked setae. Crabs in isolation exhibited the highest grooming time budget (5.22%). The presence of another conspecific decreased the grooming time budget (0.67%), and primary actions (e.g., fighting, displaying, mating) became priority. Ablation of a gill-grooming appendage did not impact fouling on gills. Grooming as a secondary action was supported. Reasons for not grooming body regions with hooked setae were discussed. Spider crabs had a lower time budget for grooming compared to most decapods, but similar to another brachyuran.
The setal abundances and distributions of the spider crab Libinia are examined, using two species. These spider crabs decorate their bodies with environmental materials and camouflage from predators. These decorations attach to hooked setae, but other types setae are prevalent in body regions where decorations occur. Adult crabs undergo a terminal molt and lose the ability to regrow setae. Little is known about setal changes over the lifetime in these crabs and if hooked setae abundance decreases with age, resulting in a loss of camouflage strategy in larger individuals. The objective of this study is to determine the prevalence and abundance of hooked and non‐hooked setae in the decorated body regions and if these setal patterns vary by species and body size. Scanning electron microscopy is used along with computer software to describe, count, and measure the setal coverage of hooked and non‐hooked setae in body regions. Small individuals have more hooked setae than larger individuals and the two species have different setal abundances of hooked and non‐hooked setae. Non‐hooked setae cover much surface areas of crabs, attach decorations, and remain on the crabs even when hooked setae are damaged and broken. Setal morphologies and fouling are described among different sized crabs and the two species, with setal types and morphologies being similar but fouling being different. Large individuals likely employ a different camouflage strategy than small individuals due to losing hooked setae but retaining non‐hooked setae.
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