Habitat partitioning between prey soldier crab Mictyris brevidactylus and predator fiddler crab Uca perplexa

Interaction and habitat partition between the soldier crab Mictyris brevidactylus (prey) and the fiddler crab Uca perplexa (predator) were examined at a sandy tidal flat on Okinawa Island, Japan, where they co-occur. Both live in dense colonies. When the soldier crabs were released in the densely populated habitat of the fiddler crab, male fiddler crabs, which maintain permanent burrows in hard sediment, preyed on small soldier crabs and repelled large ones. Thus, the fiddler crabs prevented the soldier crabs from trespassing. It was also observed whether soldier crabs burrowed successfully when they were released 1) where soldier crab burrows just under the sand were abundant, 2) in a transition area between the two species, 3) an area without either species, and 4) where artificial tunnels simulated soldier crabs' feeding tunnels were made by piling up sand in the area lacking either species. In contrast to the non-habitat area, many soldier crabs burrowed in the sediment near the release point in the tunnel, transition and artificial tunnel areas. This indicates that the feeding tunnels on the surface attracted other crabs after emergence. When the large male fiddler crabs were transplanted into the artificial burrows made in soft sediment of the soldier crab habitat, all left their artificial burrows by 2 days. In the fiddler crab habitat, however, about one-third of the transplanted male fiddler crabs remained in the artificial burrows after 3 days. The soldier crabs regularly disturb the sediment by the up and down movement of their burrow (small air chamber) between tides. This disturbance probably prevents the fiddler crab from making and occupying permanent burrows. Thus, it appears that these crabs divide the sandy intertidal zone by sediment hardness and exclude each other by different means.     

The waiting game: a "battle of waits" between predator and prey

Many prey respond to the presence of a predator by retreatinginto a shell or burrow, or by taking refuge in some other waythat guarantees their safety but restricts further informationfrom being obtained about the predator's continued presence.When this occurs, the individual predator and prey involvedbecome opponents in a "waiting game." The prey must decide howlong to wait for the predator to depart before re-emerging andpotentially exposing itself to attack. The predator must decidehow long to wait for the prey to re-emerge before departingin search of other foraging opportunities. I use a numericalapproach to determine the evolutionarily stable waiting strategyof both players and examine the effects of various parameterson the ESS. The model predicts that each player's waiting distribution—thedistribution of waiting times one would expect to observe forindividuals in that role—will have a characteristic shape:the predator's distribution should resemble a negative exponentialfunction, whereas the waiting time of the prey is predictedto be more variable and follow a positively skewed distribution.The model also predicts that very little overlap will occurbetween the players' waiting distributions, and that the predatorwill rarely outwait the prey. Empirical studies relating tothe model and comparisons between the waiting game and the asymmetricwar of attrition are discussed.     

The SW Atlantic burrowing crab Chasmagnathus granulatus Dana affects the distribution and survival of the fiddler crab Uca uruguayensis Nobili

In this paper, we address the question of whether the presence of the burrowing crab Chasmagnathus granulatus affects the habitat use of the fiddler crab Uca uruguayensis. Field samples showed that the species have a disjoint spatial distribution. Male fiddler crab density decreased in zones with C. granulatus, however, female density increased. Male fiddler crabs avoided feeding on sediment affected by C. granulatus and were more preyed. Predation was higher during the fiddler crab reproductive season and, probably due to predation risk, males showed lower reproductive display in shared zones. Field experiments shows that when C. granulatus were excluded, densities of U. uruguayensis increased mainly due to an increase in density of males. Habitat differentiation of these species may be because C. granulatus affects U. uruguayensis in several ways, including direct predation, disturbance and behavioural changes associated to predation risk. Males and females are affected differentially probably because of the extreme sexual dimorphism of this crab species. Coloration on enlarged claw and waving activities are all factors that increase predation risk for male and the presence of only one feeding claw may increase sediment-mediated effects.     

Shell use by juvenile fiddler crabs Uca pugnax and U. pugilator

The present study documents for the first time shell use by juvenile fiddler crabs in the salt marsh. Twenty visits were made to six salt marsh sites at Tybee Island, Georgia between 2007 and 2009. One hundred empty Littorina irrorata shells were collected at each site on each field trip. Juvenile carapace width was measured, crabs sexed, and species identification completed using RFLP analysis. Shell use of up to 79% was observed. Two species of fiddler crabs were found in empty shells, Uca pugnax and U. pugilator. U. pugnax was the dominant species at all sites representing 62-84% of the juvenile fiddler crab population. Juvenile sex ratios were female-biased (1.7:1) at all six sites. Juvenile size did not vary significantly between species but males of both species were significantly larger than females. Size frequency distribution of carapace width revealed that shell use varied with size and sex. In the 3 to 4 mm size class, juvenile females outnumbered juvenile males in empty L. irrorata shells while in the 5 to 6 mm size class and greater, juvenile males outnumbered juvenile females in shells. Significantly more juvenile fiddler crabs were found in empty shells during flood than ebb tide at 3 of the sites. This discovery illuminates the resourcefulness of juvenile fiddler crabs and provides another mechanism that might enhance survival.     

Optimal foraging versus shared doom effects: interactive influence of mussel size and epibiosis on predator preference

In the western Baltic Sea, the highly competitive blue mussel Mytilus edulis tends to monopolize shallow water hard substrata. In many habitats, mussel dominance is mainly controlled by the generalist predator Carcinus maenas. These predator-prey interactions seem to be affected by mussel size (relative to crab size) and mussel epibionts.There is a clear relationship between prey size and predator size as suggested by the optimal foraging theory: Each crab size class preferentially preys on a certain mussel size class. Preferred prey size increases with crab size.Epibionts on Mytilus, however, influence this simple pattern of feeding preferences by crabs. When offered similarly sized mussels, crabs prefer Balanus-fouled mussels over clean mussels. There is, however, a hierarchy of factors: the influence of attractive epibiotic barnacles is weaker than the factor ‘mussel size’. Testing small mussels against large mussels, presence or absence of epibiotic barnacles does not significantly alter preferences caused by mussel size. Balanus enhanced crab predation on mussels in two ways: Additional food gain and, probably more important, improvement in handling of the prey. The latter effect is illustrated by the fact that artificial barnacle mimics increased crab predation on mussels to the same extent as do live barnacles.We conclude that crab predation preferences follows the optimal foraging model when prey belong to different size classes, whereas within size classes crab preferences is controlled by epibionts.     

Sexual selection and the physiological consequences of habitat choice by a fiddler crab

In mid-Atlantic salt marshes, reproductively active male sand fiddler crabs, Uca pugilator, use a single greatly enlarged major claw as both a weapon to defend specialized breeding burrows from other males and an ornament to attract females for mating. During the summer breeding season, females strongly prefer to mate with males controlling burrows in open areas high on the shore. Food availability decreases while temperature and desiccation stress increase with increasing shore height, suggesting that the timing and location of fiddler crab mating activity may result in a potential trade-off between reproductive success and physiological condition for male crabs. We compared thermal preferences in laboratory choice experiments to body temperatures of models and living crabs in the field and found that from the perspective of a fiddler crab, the thermal environment of the mating area is quite harsh relative to other marsh microhabitats. High temperatures significantly constrained fiddler crab activity on the marsh surface, a disadvantage heightened by strongly reduced food availability in the breeding area. Nevertheless, when the chance of successfully acquiring a mate was high, males accepted a higher body temperature (and concomitantly higher metabolic and water loss rates) than when the chances of mating were low. Likewise, experimentally lowering costs by adding food and reducing thermal stress in situ increased fiddler crab waving display levels significantly. Our data suggest that fiddler crabs can mitigate potential life history trade-offs by tuning their behavior in response to the magnitude of both energetic and non-energetic costs and benefits.     

Quantitative analysis of fiddler crab flock movement: evidence for ‘selfish herd’ behaviour

The selfish herd hypothesis predicts that aggregations form because individuals move towards one another, and that this movement will minimize predation risk as measured by the domain of danger. To test the predictions of the selfish herd hypothesis in the field, we videotaped the movements of sand fiddler crab, Uca pugilator, flocks being attacked by predators. After recording 12 attacks on crabs by shorebird and human attackers, we digitized the video, and determined the positions of crabs before and after being frightened. We estimated the time of panic initiation by the rapid increase in the crabs' velocity. Crab flocks became more cohesive after panic initiation. The frequency distribution of the crabs' domains of danger shifted significantly towards smaller domains after panic initiation. The median domain of danger was significantly lower after panic initiation than beforehand. Two other indices of aggregation also showed statistically significant increases in flock cohesion following panic initiation. We conclude that fiddler crab behaviour is consistent with the selfish herd hypothesis. Therefore, our results support the selfish herd hypothesis as an explanation for gregarious behaviour. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.     

A Spatially Explicit Model of Synchronization in Fiddler Crab Waving Displays

Fiddler crabs (Uca spp., Decapoda: Ocypodidae) are commonly found forming large aggregations in intertidal zones, where they perform rhythmic waving displays with their greatly enlarged claws. While performing these displays, fiddler crabs often synchronize their behavior with neighboring males, forming the only known synchronized visual courtship displays involving reflected light and moving body parts. Despite being one of the most conspicuous aspects of fiddler crab behavior, little is known about the mechanisms underlying synchronization of male displays. In this study we develop a spatially explicit model of fiddler crab waving displays using coupled logistic map equations. We explored two alternative models in which males either direct their attention at random angles or preferentially toward neighbors. Our results indicate that synchronization is possible over a fairly large region of parameter space. Moreover, our model was capable of generating local synchronization neighborhoods, as commonly observed in fiddler crabs under natural conditions.     

Temperature influences the reproduction of fiddler crabs at the southern edge of their distribution

Understanding the spatial patterns of reproductive biology might provide predictions about fitness and population stability in different locations within the geographical range of a particular species. Leptuca uruguayensis is a fiddler crab that breeds year round in tropical estuaries but only in summer months in temperate salt marshes. In this study, we examined several reproductive attributes of the southernmost population of L. uruguayensis, including the proportion of ovigerous females, the proportion of surface‐active crabs, the developmental status of the gonads and hepatopancreas, and the fullness of seminal receptacles, and related them to environmental factors such as temperature, photoperiod, and sediment organic matter content. We found that temperature was the environmental factor that was most correlated with the reproductive process of the southernmost fiddler crab, since this environmental factor was related to ovarian development, to the fullness of seminal receptacles, and to the hepatosomatic index. At the southern edge of its distribution, the low temperatures of winter restricted reproduction in L. uruguayensis. These winter temperatures might represent the lower limit of the thermal window of this fiddler crab, limiting its extension toward higher latitudes.     

Hiding behaviour in fiddler crabs: how long should prey hide in response to a potential predator?

Do predator-prey ‘waiting games’ where prey hide from potential predators have inherently unstable evolutionary outcomes, making it impossible to generate quantitative predictions about hiding times? Fiddler crabs, Uca lactea perplexa, respond to potential predators by retreating into their burrows. Time inside the burrow during unprovoked retreats during normal activity provides a ‘null model’ to test whether sex, tidal cycle and body size affect hiding time from potential predators. Using experimentally created predator-like stimuli we found that males hid for significantly longer than females, and larger crabs of both sexes also hid for longer. This differs from burrow use during unprovoked retreats, suggesting hiding time varies depending on the potential risk of predation on re-emergence. If risk prior to hiding predicts risk on emergence, the closer the proximity of a predator-like stimulus when first encountered the longer crabs should hide. We confirmed this experimentally (stimuli at 0.5 versus 2.5 m). Finally, we tested whether males hide for longer when a predator-like stimulus approaches them directly rather than tangentially. None of three pairwise comparisons was statistically significant, but crabs hid less as the angle of approach became more tangential. These results suggest prey can use stimuli prior to hiding to predict predation risk on re-emergence, but studies on predators are required to test this claim. Finally, theoretical models must explain why hiding time has a lognormal distribution and low variance such that a predator can predict when most prey will re-emerge. For example, 95% of crabs re-emerged within 2.3 min of hiding. Copyright 2003 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour.      

Predator-prey dynamics between recently established stone crabs (Menippe spp.) and oyster prey (Crassostrea virginica)

Range expansion and population establishment of individual species can have significant impacts on previously established food webs and predator-prey dynamics. The stone crab (Menippe spp.) is found throughout southwestern North Atlantic waters, from North Carolina through the Gulf of Mexico and the Central American Caribbean, including the Greater Antilles. Recent observations suggest that stone crabs have become better established on certain oyster reefs in North Carolina than in the early 1900s when they we first observed in NC. To assess the predatory impact of stone crabs on oysters, we (1) quantified stone crab densities on subtidal oyster reefs in Pamlico Sound, NC using scuba surveys, and (2) conducted laboratory predation experiments to assess the functional response of stone crabs to varying densities of oysters. We then (3) analyzed previously unpublished functional response data on another important oyster predator, the mud crab Panopeus herbstii. Finally, we (4) compared and contrasted potential predatory impacts of stone, mud and blue crabs (Callinectes sapidus). The functional response data and analyses for both stone crabs and mud crabs were consistent with a type II functional response. Mud crabs, on a m² basis, inflicted the highest proportional mortality on oysters over a 24 hour period, followed by stone and then blue crabs. Proportional mortality did not vary significantly with oyster size; however, relatively small and large oysters were consumed disproportionately less than medium-sized oysters, likely due to the mechanical inability of stone crabs to handle small oysters, and the inability to crush large oysters. Although stone crabs appear to be established in Pamlico Sound at densities equivalent to densities in other systems such as the U.S. Florida Panhandle, their predatory activities on oysters are not expected to have as significant a negative impact on oyster populations compared to other resident predators such as mud crabs.     

Impact of fiddler crab foraging and tidal inundation on an intertidal sandflat: season-dependent effects in one tidal cycle

Intertidal sandflats inhabited by fiddler crabs are ideal systems in which to study the effects of physical and biological processes. This study addressed two questions: (1) Do fiddler crab feeding and tidal inundation have measurable effects on the sandflat over one tidal cycle? (2) Does the sandflat change over the course of a year? In field exclusion/inclusion experiments, fiddler crabs reduced sediment organic content by 40%, Chlorophyll a levels by 20% and meiofaunal density by 60% in one tidal cycle. Effects were most pronounced in the spring when organic content and meiofaunal densities were maximal. Effects of foraging were not erased by the tide and accumulated over time. The sandflat had highest levels of all variables in spring and minimal levels during summer and fall. Crabs graze the sandflat to minimum levels in the spring. Due to crab foraging, the flat is barren during the summer and fall, and recovers during the winter when crabs are minimally active.     

Adaptive significance of hatching rhythms and dispersal patterns of estuarine crab larvae: avoidance of physiological stress by larval export?

Estuarine crabs commonly display two larval dispersal patterns in which larvae are either exported from or retained within estuaries. The semiterrestrial fiddler crab Uca minax (LeConte, 1855) hatches on nocturnal spring high tides in the upper estuary and larvae are rapidly transported downstream. The mud crab Rhithropanopeus harrisii (Gould, 1841) hatches on nocturnal high tides of any amplitude and larvae are retained behaviorally in the upper estuary throughout development. If larvae are exported from the estuary to avoid environmental stress, then exported larvae should be less tolerant of high temperatures and low salinities than retained larvae. Larvae of these two species of estuarine crabs were hatched at 20‰ and 25 °C and subjected to salinities of 0, 5, 10,20, and 30‰, temperatures of 25 and 35 °C, and exposure times of 2, 6, 12, and 48 h. Larvae of both species reared at 30 or 20‰ survived well, while those reared in fresh water all died within 2 h regardless of temperature. Mud crab larvae reared at 5 and 10‰ survived better at the lower temperature (25 °C), higher salinity, and shorter exposure times. There was no significant effect of temperature or salinity on the survival of fiddler crab larvae, although survival decreased with increasing exposure time. Thus, the hypothesis that fiddler crab larvae are exported into stable coastal waters to reduce physiological stress is not supported. However, fiddler crab larvae may have evolved to be very tolerant of extreme temperature and salinity stress because they, unlike mud crabs, often release their larvae into shallow creeks. Most fiddler crab larvae are released on nocturnal spring high tides, which facilitates dispersal from tidal creeks. However, freshwater runoff and heat transferred from the marsh surface to flooding waters may still create stressful conditions for larvae soon after they are released. Larval release on spring high tides may facilitate dispersal from tidal creeks.     

Coupling between microphytobenthic biomass and fiddler crab feeding

Among the organic matter ingested by fiddler crabs, microphytobenthos is of fundamental importance because it is their main N source. Microphytobenthos abundance generally develop semilunar changes as the dynamics of tidal exposures and day-night cycle are not held constant across days, modifying the balance between growth and mortality. In this study we explored the coupling between temporal dynamics in microphytobenthos abundance and crab feeding activity. We measured the Chlorophyll a content in the 2 mm surficial sediment surrounding the burrows and the crab feeding activity over two semilunar cycles. Chlorophyll a and crab feeding activity showed biweekly cyclic dynamics. Crabs did not concentrate feeding activity around days with maximum abundance of microhytobenthos. This phase difference between both dynamics could be the result of the crab feeding impact, but a crab experimental exclusion showed that the temporal dynamics of Chlorophyll a content stayed unchanged when feeding activity was removed. Comparisons between fed and unfed sediment suggest that the feeding efficiency changes with tidal dynamic. Crabs achieved more than 50% of Chlorophyll a extraction during days of highest feeding activity, and less than 30% during days of low feeding activity or low microhytobenthos abundance. Furthermore, comparisons of fed sediment between consecutive days indicated that Chlorophyll a was completely replenished during days with high flooding tides, but partially replenished during days near neap tides. Environmental conditions affecting feeding efficiency may select crabs to concentrate feeding activity before days with the highest microhytobenthos abundance. The low feeding impact on microphytobenthos dynamics suggests that fiddler crabs would not control microhytobenthos abundance and thus unable to absorb the increasing eutrophication of studied estuarine areas.     

Determination of Key Environmental Factors Responsible for Distribution Patterns of Fiddler Crabs in a Tropical Mangrove Ecosystem

In tropical regions, different species of fiddler crabs coexist on the mangrove floor, which sometimes makes it difficult to define species-specific habitat by visual inspection. The aim of this study is to find key environmental parameters which affect the distribution of fiddler crabs and to determine the habitats in which each species was most abundant. Crabs were collected from 19 sites within the mudflats of Sepang-Lukut mangrove forest. Temperature, porewater salinity, organic matter, water content, carbon and nitrogen content, porosity, chlorophyll content, pH, redox potential, sediment texture and heavy metals were determined in each 1 m² quadrate. Pearson correlation indicated that all sediment properties except pH and redox potential were correlated with sediment grain size. Canonical correspondence analysis (CCA) indicated that Uca paradussumieri was negatively correlated with salinity and redox potential. Sand dwelling species, Uca perplexa and Uca annulipes, were highly dependent on the abundance of 250 μm and 150 μm grain size particles in the sediment. Canonical Discriminative Analysis (CDA) indicated that variation in sediment grain size best explained where each crab species was most abundant. Moreover, U. paradussumieri commonly occupies muddy substrates of low shore, while U. forcipata lives under the shade of mangrove trees. U. annulipes and U. perplexa with the high number of spoon tipped setae on their second maxiliped are specialized to feed on the sandy sediments. U. rosea and U. triangularis are more common on muddy sediment with high sediment density. In conclusion, sediment grain size that influences most sediment properties acts as a main factor responsible for sediment heterogeneity. In this paper, the correlation between fiddler crab species and environmental parameters, as well as the interaction between sediment characteristics, was explained in order to define the important environmental factors in fiddler crab distributions.     

Density affects mating mode and large male mating advantage in a fiddler crab

Fiddler crabs show two different mating modes: either females search and crabs mate underground in male burrows, or males search and crabs mate on the surface near female burrows. We explored the relationship between crab density, body size, the searching behavior of both sexes, and the occurrence of both mating modes in the fiddler crab Uca uruguayensis. We found that crabs change their mating mode depending on their size and crab density. Crabs mated mostly on the surface at low densities, and underground at high densities. The proportion of wandering receptive females but not courting males accounted for the variation in mating modes. This suggests that whether crabs mate underground (or on the surface) is determined by the presence (or absence) of searching females. We found that the change in the mating mode affected the level of assortative mating; males mating underground were bigger than those mating on the surface, suggesting active female choice. Given that fiddler crabs experience multiple reproductive cycles, they are prone to showing behavioral plasticity in their mating strategy whenever the payoffs of using different mating modes differ between reproductive events. Our results suggest that the incorporation of different levels of environmental variability may be important in theoretical models aimed at improving our understanding of the evolution of alternative mating tactics and strategies.     

Independent and interactive effects of two facilitators on their habitat‐providing host plant,Spartina alterniflora

The role of habitat‐providing species in facilitating associated species abundance and diversity is recognized as a key structuring force in many ecosystems. Reciprocal facilitation by associates, often involving multiple species, can be important for the maintenance of the host species. As with other multi‐species interactions (e.g. multiple predator effects), non‐additive relationships may be common among these associates, yet relatively few studies have examined potential interactions among multiple facilitator species. We combined field surveys and a mesocosm experiment to examine the independent and interactive effects of two co‐occurring facilitator species, ribbed mussels Geukensia demissa and fiddler crabs Uca pugilator, on their host salt marsh plant species, cordgrass Spartina alterniflora. We also experimentally examined how these relationships varied across different host plant genotypes. Overall, facilitator effects increased with increasing facilitator density. There was a significant interaction between mussel and fiddler crab presence, indicating that the effects of each species on cordgrass were dependent on the presence of the other facilitator species. In addition, there were strong interactions among mussels, fiddler crabs, and plant genotype, with greater variation in the performance of individual genotypes when fiddler crabs were absent. Our work reinforces the importance of considering multiple responses when assessing the functional redundancy of co‐occurring facilitators, as species are seldom completely redundant across the range of services they provide. It also highlights that the strength and direction of species interactions can vary due to genetic variation within the interacting species.     

The relative importance of substratum characteristics and recruitment in determining the spatial distribution of the fiddler crab Uca uruguayensis Nobili

The roles of sediment characteristics and the pattern of recruitment in influencing the abundance of the fiddler crab Uca uruguayensis on Argentinean mudflats were evaluated. The density of adult crabs showed a patchy distribution related to the sediment thickness (depth at which a layer of fossil shells are buried), but the density of juvenile crabs was not coupled with the density of adult crabs. In a field experiment, fossil shells were removed and the density of crabs significantly increased, which demonstrates that the presence of the layer of shells is a structure that may hinder the establishment of burrows. The density of crabs was related to sediment thickness, sediment torque and organic matter content. The importance of each of these variables was different for adult and juvenile crabs, indicating that the distribution of adult crabs may be caused by mechanisms affecting adult crabs themselves and is not established by the recruitment pattern. Moreover, in a field experiment, the density of juveniles decreased when adult crabs were added, and increased when adult crabs were removed.The morphology of burrows was related to sediment characteristics. Burrows were deeper, longer and more voluminous when sediment thickness was high. The volume of burrows decreased with increasing sediment torque. These results suggest that the morphology of burrows is related to the space available and the ease with which sediment it can be excavated. However, an important amount of variability remained unexplained, suggesting the presence of additional environmental variables or behavioural plasticity not considered by this study. Together, these results demonstrate that the spatial heterogeneity in the environmental factors can be translated to a spatial heterogeneity in the distribution of fiddler crabs.     

Composition and abundance of shorebird and macroinvertebrate communities differ according to densities of burrowing fiddler crabs in tropical intertidal flats

The burrowing activity of fiddler crabs inhabiting intertidal flats creates visually distinct patches within these habitats. However, differences in the composition and abundance of shorebirds and their macroinvertebrate prey between areas inhabited or not by crabs are yet to be studied. Here, we compare the macroinvertebrate and shorebird assemblages in low and high crab density areas in the intertidal flats of the Bijagos archipelago, Guinea-Bissau. High crab density areas are associated with lower richness and densities of macroinvertebrates. Shorebird assemblages were also less rich at high crab density areas and the differences in species composition occurred according to prey type preferences. Fiddler crab density was the most important variable explaining macroinvertebrate abundance, after accounting for the effects of fine fraction of sediment and distance to coast. Nonetheless, a controlled experimental setup would be required to attribute differences found to the engineering activity of fiddler crabs rather than other unaccounted habitat features. Our findings suggest that crab patches should be taken into account when assessing the distribution and abundance of macroinvertebrates and shorebirds in intertidal areas. Since low and high crab density areas differ markedly in terms of shorebird carrying capacity, monitoring variations in their extent will be important to interpret past and present population trends.

     

Morphological diversity of setae on the second maxilliped of fiddler crabs (Decapoda: Ocypodidae) from the southwestern Atlantic coast

Fiddler crabs are deposit feeders, and use the setae on their mouth appendages to manipulate sediment particles to extract food. The number of spoon‐tipped setae on the second maxilliped is frequently related to the distribution of fiddler crabs on estuarine sediments, but no study has compared the morphological diversity of these setae among multiple fiddler crab species. Here, we describe and classify the setae of the second maxillipeds of the nine Uca spp. known from the Brazilian coast. The second maxilliped of each species was examined by scanning electron microscopy. Six types of setae (five papposerrate, and one pappose) were described on the meropodite of the second maxilliped. Among the papposerrate setae, one type had a spoon‐like tip, and the morphology of this type, especially the degree of curvature, differed between species. Members of Uca leptodactylus, U. uruguayensis, and U. maracoani had highly concave spoon‐tipped setae. In U. rapax and U. cumulanta, the setal tip was moderately curved, while in U. thayeri, U. burgersi, and U. mordax, this curvature was slight. At the other extreme, the meropodite of the second maxilliped of U. vocator lacked setae altogether. This is the first study that describes differences in the degree of curvature of spoon‐tipped setae in fiddler crabs. This trait may be strongly related to the distribution of these fiddler crabs on different estuarine substrates.