Locomotor Rhythms in the Fiddler Crab, Uca subcylindrica

The locomotor activities of individual specimens of Uca subcylindrica (Stimpson) collected from semi-arid, supratidal habitats in south Texas and northeastern Mexico were studied in the laboratory using periodogram analysis. When crabs were placed under constant darkness (DD) or constant illumination (LL), free-running circadian rhythms were observed in the activity recordings. The locomotor activity of strongly rhythmic crabs in LL has an average period length of 24.4 h. Crabs held in DD express motor rhythms with periods of approximately 24.0 h. In LL the most common wave form for activity is unimodal, while under DD it is bimodal. Recordings under natural illumination (NL) revealed that both period length and the time of maximum activity (phasing) varied through the year. During winter months, the crabs are primarily diurnal with peaks in activity occurring between 0900 and 2100 h and possess a circadian rhythm with a 23.9 h period. During summer, crabs were nocturnal with maximal activity between 1300 and 0600 and a circadian period closer to 24.0 h. In these experiments, the rhythmic locomotor activities of U. subcylindrica are best described as “circadian”. This is unusual for a genus known for its expression of circatidal and circalunidian rhythms.     

Locomotor Rhythms in the Fiddler Crab,Uca subcylindrica

The locomotor activities of individual specimens of Uca subcylindrica (Stimpson) collected from semi-arid, supratidal habitats in south Texas and northeastern Mexico were studied in the laboratory using periodogram analysis. When crabs were placed under constant darkness (DD) or constant illumination (LL), free-running circadian rhythms were observed in the activity recordings. The locomotor activity of strongly rhythmic crabs in LL has an average period length of 24.4 h. Crabs held in DD express motor rhythms with periods of approximately 24.0 h. In LL the most common wave form for activity is unimodal, while under DD it is bimodal. Recordings under natural illumination (NL) revealed that both period length and the time of maximum activity (phasing) varied through the year. During winter months, the crabs are primarily diurnal with peaks in activity occurring between 0900 and 2100 h and possess a circadian rhythm with a 23.9 h period. During summer, crabs were nocturnal with maximal activity between 1300 and 0600 and a circadian period closer to 24.0 h. In these experiments, the rhythmic locomotor activities of U. subcylindrica are best described as “circadian”. This is unusual for a genus known for its expression of circatidal and circalunidian rhythms.     

Regeneration of Walking Legs in the Fiddler Crab Uca pugilator

SYNOPSIS. Regeneration of walking legs in the fiddler crab Ucapugilator is most efficient when it follows autotomy (the reflexiveloss of a limb). Closure of the wound and would healing occurimmediately following autotomy and visible regeneration beginswithin a few days. Regeneration of the walking leg occurs intwo distinct stages: The first stage, called Basal Growth, involvesmitosis and differentiation. The second stage involves primarilyprotein synthesis and water uptake and is called ProecdysialGrowth. Proecdysial Growth is, in part, under direct hormonalstimulation.     

Female Choice in the Synchronously Waving Fiddler Crab Uca annulipes

In the fiddler crab, Uca annulipes, males attract receptive females into their burrows by waving their greatly enlarged major claw. We have previously shown that males clustered around a female wave in close synchrony. Females may have a preference for leading signals and synchronised waving may arise as an epiphenomenon of competition between males to signal first. Indeed, the males in clusters that females approach and visit in their burrows are more likely to produce leading waves than are their neighbours. Here we document two other differences in the waving behaviour of visited males and their neighbours. First, visited males complete the downward component of the wave more rapidly than their neighbours. Second, the interval between the end of one wave and the start of the next is shorter for visited males. How can waving be synchronous if visited males wave faster than their neighbours? While only 9% (40/431) of waves by neighbours did not overlap those of the visited male, 22% (110/501) of visited male waves did not overlap the wave of a focal neighbour (111 visited male-neighbour dyads). Hence, while overlapping waves are nearly synchronous, visited males produce additional, ‘nonoverlapping’ waves that result in a higher wave rate than that of their neighbours.     

Hormonal Control of the Molt Cycle in the Fiddler Crab Uca pugilator

Comparison of the circulating steroids in the blood of crabslacking neurosecretory eyestalk centers and crabs with thosecenters intact (but lacking several walking legs) has revealeddifferences in vivo that can be attributed to eyestalk factors.It is concluded that eyestalk factors (including the putativemolt-inhibiting hormone, MIH): 1) exert control in vivo overproduction of 25-deoxyecdysone by the crab Y-organ, 2) controlcyclic steroid production throughout anecdysis and parts ofproecdysis and 3) are not solely responsible for the increasedsteroid production that occurs during late proecdysis. Usingthe data presented here and previously published data, a simplefeedback model for the control of Y-organ activity is proposed.The model suggests that the Y-organs of the crabUca pugilatorare modestly active during anecdysis but become further activatedduring late proecdysis. The increased activation requires morethan eyestalk removal and may involve additional extra-eyestalkfactors.     

Limb Regeneration in the Fiddler Crab, Uca pugilator: Histological, Physiological and Molecular Considerations

This paper summarizes our recent work on the histological, physiologicaland molecular aspects of limb regeneration in the fiddler crabUca pugilator and new information is presented on mitotic activityin the blastema during the first days of blastemal organization.We also report for the first time the localization of vertebrategrowth factor immunoreactivity (FGF 2 and FGF 4) in the regeneratingblastema. In the first part of this paper we review recent histologicalfindings concerning the physical events that accompany autotomyof limbs and propose a new function for the autotomy membrane—thetethering of the regenerating pedal nerve to the walls of thecoxa. In the second part of the paper we review our recent findingson the identification and characterization of the Uca ecdysteroidreceptor (UpEcR, and its potential dimer partner, the retinoid-X-receptor,UpRXR). Using Uca-specific antibody probes raised in our lab,we have been able to identify specific cells in the early blastemathat express receptor proteins. The regenerating limb of thefiddler crab is responsive to both steroids and retinoids andmRNA for steroid and retinoid receptors are expressed in theregenerating limb buds during all stages of regeneration. TheDNA and deduced amino acid sequences of the ecdysteroid receptoris very similar to the sequences of insect EcRs, while the retinoidreceptor is similar to insect protein (ultraspiracle) in theDNA-binding domain, but closer to vertebrate RXRs in the ligandbinding domain     

Limb Regeneration in the Fiddler Crab, Uca pugilator: Hormonal and Growth Factor Control

This paper summarizes recent work on various aspects of hormonalcontrol of regeneration in the crustacean, Uca pugilator. Hormonalcontrol in this crab is effected by means of the crustacteansteroid hormones, the ecdysteroids. New evidence is presentedsupporting a role for the retinoid hormones, all-trans retinoicacid and 9-cis retinoic acid, in the control of regenerationin these animals. The possible role of fibroblast growth factorsin organization of the limb blastema is explored and the similaritiesbetween vertebrate and invertebrate control of regenerationare discussed.     

Locomotor Activity of the Fiddler Crab,Uca subcylindrica (Stimpson), under Artificial Illumination

Specimens of the fiddler crab Uca subcylindrica (Stimpson) were captured in south Texas (USA) for locomotor rhythm studies. Actographic data were analyzed using Tau? sofware. Under constant illumination (LL) and darkness (DD), the semiterrestrial crabs express a circadian rhythm of locomotion. When exposed to illumination/darkness cycles (LD_12:12 or LD_14:10), their bouts of activity are entrained to the photoperiod. In LD, activity is generally bimodal with an initial burst about 0.5 h after illumination. A second burst of activity begins 1 to 2 h before the end of illumination. When transferred from LD to LL, a locomotor rhythm with an average period of 24.6 ± 1.0 h (n = 19) is expressed in 89 percent of the crabs. On the other hand, when placed in DD after LD (n = 8), the crabs are either arrythmic or weakly rhythmic (period = 23.8 ± 0.2 h; n = 2). If the onset of illumination is advanced by 6 h, a period of less than 24.0 h is detected in the actogram. If the onset of illumination is delayed by 6 h, a locomotor rhythm with a period greater than 24.0 h appears. The locomotor behavior of this species of fiddler crab, Uca subcylindrica, is not related to the tidal rhythmicities seen in other members of the genus Uca. Rather, it has strong circadian components.     

Locomotor Activity of the Fiddler Crab, Uca subcylindrica (Stimpson), under Artificial Illumination

Specimens of the fiddler crab Uca subcylindrica (Stimpson) were captured in south Texas (USA) for locomotor rhythm studies. Actographic data were analyzed using Tau™ sofware. Under constant illumination (LL) and darkness (DD), the semiterrestrial crabs express a circadian rhythm of locomotion. When exposed to illumination/darkness cycles (LD_12:12 or LD_14:10), their bouts of activity are entrained to the photoperiod. In LD, activity is generally bimodal with an initial burst about 0.5 h after illumination. A second burst of activity begins 1 to 2 h before the end of illumination. When transferred from LD to LL, a locomotor rhythm with an average period of 24.6 ± 1.0 h (n = 19) is expressed in 89 percent of the crabs. On the other hand, when placed in DD after LD (n = 8), the crabs are either arrythmic or weakly rhythmic (period = 23.8 ± 0.2 h; n = 2). If the onset of illumination is advanced by 6 h, a period of less than 24.0 h is detected in the actogram. If the onset of illumination is delayed by 6 h, a locomotor rhythm with a period greater than 24.0 h appears. The locomotor behavior of this species of fiddler crab, Uca subcylindrica, is not related to the tidal rhythmicities seen in other members of the genus Uca. Rather, it has strong circadian components.     

Pillar Function in the Fiddler Crab Uca beebei (II): Competitive Courtship Signaling

Male Uca beebei court and attract females into burrows they defend on muddy sand flats in the intertidal zone on the Pacific coast of the tropical Americas. Mating, oviposition and incubation (breeding) occur underground in males' burrows. Some courting males build mud pillars (2 cm high) at the entrance of their burrow. The purpose of this field study was to assess the role of pillars in competitive courtship signaling among males. I studied the effect of pillars on female behavior by recording the responses of wandering females to courtship from males resident at burrows with and without pillars. I also caught females, released them individually in a circular arena with an equal number of empty burrows with and without pillars around its circumference, and chased the females with a simulated avian predator. Females moved to burrows of both types more often when they were courted (82%) than when they were chased (67%). Receptive females were attracted to the burrows of the males that courted them significantly more often (97%) when these burrows had pillars than when they lacked pillars (66%). However, once females entered males' burrows they were equally likely to remain, mate and breed in both types of burrows. Females also more often moved to burrows with pillars (66%) than to burrows without pillars when they ran from the simulated predator. Both male courtship displays and pillars probably provide cues females use to locate males' burrows. The visual similarity between pillars and a display courting males give immediately before they enter their burrows suggests that pillars are icons of the display. The effect of pillars on female behavior, the timing of pillar building relative to when females choose mates, and contrasts in the behavior of males that do and those that do not build pillars suggest that pillar building has evolved due to competition among males to attract females into their burrows.     

氨氮对不同生长阶段的弧边招潮急性毒性研究

在pH8.09、水温28℃±1℃、盐度5‰条件下,进行了氨氮对不同生长阶段的弧边招潮急性毒性试验。结果显示:氨氮对全甲宽小于1.5cm、1.5cm、1.5cm至2.5cm之间3个生长阶段的弧边招潮96h的半数致死浓度(LC50)分别为47.28mg·L-1、71.49mg·L-1和90.57mg·L-1,三者之间差异极显著(P<0.01),对应的非离子氨浓度为3.71mg·L-1、5.61mg·L-1和7.11mg·L-1;氨氮的安全浓度分别为4.73mg·L-1、7.15mg·L-1和9.06mg·L-1,对应的非离子氨浓度为0.37mg·L-1、0.56mg·L-1和0.71mg·L-1。结果表明,氨氮对弧边招潮的毒性与氨氮浓度和中毒时间呈正相关。3个生长阶段弧边招潮对氨氮的耐受性大小次序为:全甲宽1.5cm至2.5cm之间>全甲宽1.5cm>全甲宽小于1.5cm。     

Pillar Function in the Fiddler Crab Uca beebei (I): Effects on Male Spacing and Aggression

Males of 14 species of fiddler crabs (genus Uca) are known to build structures out of mud or sand at the entrances to burrows they court from and defend. A study of spacing, space use and aggression between courting male Uca musica (Zucker 1974, 1981) suggested that the hoods males build reduce territorial overlap and rates of aggression between neighboring males. Thus, each male may have more time to court females during limited lunar, diurnal and tidal mating periods. I studied the courtship and aggressive behavior of male Uca beebei in the field to determine if the pillars males of this species build affect male behavior as do the hoods of U. musica. U. beebei occurs sympatrically with U. musica on the Pacific coast of Panama and is broadly similar in its ecology and mating behavior. Unlike the hoods of U. musica, pillars did not focus a male's activity space away from its closest neighbor nor did they reduce either overlap with neighbors' activity spaces or rates of aggressive interaction among neighbors. Pillar builders courted more but also fought their neighbors more than did males that did not build pillars. The pillars of U. beebei and the hoods of U. musica affect male behavior differently and probably have different functions.     

Distal Retinal Pigment of the Fiddler Crab,Uca pugilator: Release of the Dark-Adapting Hormone by Methionine Enkephalin and FMRFamide

The neuropeptides methionine enkephalin and FMRFamide, when injected into intact fiddler crabs, Uca pugilator, produce dark adaptation of the distal retinal pigment. Furthermore, both neuropeptides stimulate release of distal retinal pigment dark-adapting hormone activity from the isolated eyestalk neuroendocrine complex. It is hypothesized that both neuropeptides, when injected into intact fiddler crabs, act only indirectly on the distal retinal pigment, by stimulating release of this dark-adapting hormone.     

Size-dependent Mating Behaviours of Male Sand-bubbler Crab,Scopimera globosa: Alternative Tactics in the Life History

Factors leading to the separation of mating behaviours were investigated in the sand-bubbler crab, Scopimera globosa. The crabs mated on the surface (surface copulation, SC) and underground (UC). UC males were large (old) whilst SC males were small (young). Burrowless females bred in the UC males' burrows. These females accepted UC in exchange for access to a burrow. UC occurred much more frequently than SC in the burrow area in which females oviposited. Most SC occurred in the water-saturated area affording a rich diet. SC was accepted by most large and small females in both areas and most UC by small females in the burrow area. SC was an alternative to UC for males in that there was a size dependence between types of copulation. These two mating behaviours involved different degrees of interaction with neighbouring males. Males attempting to carry a female to their burrows for UC were more often disturbed by other males than were males attempting SC. In the interaction for both UC and SC, larger males were likely to resist the disturbances. UC males needed their own burrows, but these burrows were not enlarged before mating. UC males have a higher paternity of eggs than SC males, because SC males' sperm is often displaced by other males. Thus, UC was a behaviour with relatively higher costs and benefits for male crabs than SC behaviour. Alternative mating behaviours in male S. globosa are conditional, and explained by intrasexual interactions and a male life history strategy with a trade-off between growth and reproduction. It is not likely that the size dependence of male mating behaviour is caused by mate preference of females for UC males in the burrow area.     

Behavior of Four Species of Fiddler Crabs,Genus Uca,in Southeast Sulawesi,Indonesia

We studied the behaviors of four species of sympatric fiddler crabs on Kaledupa Island, Indonesia. Species differences in activity level, grooming, burrowing and feeding were related to their habitat and food. Uca chlorophthalmus, living in muddy mangrove areas, were inactive and spent most of the time feeding in place. Females fed 50% faster than males and spent more time feeding. U. vocans was the dominant species at the beach in silty sand and was very active. Its feeding rate was about twice that of the former species, females fed more rapidly than males, and many crabs of both sexes fed in droves at the water’s edge during ebb tides. During ebb tides, they spent most of their time feeding, while at flood tide they engaged in a greater variety of activities, including burrow maintenance. They frequently walked while feeding and interacted aggressively. U. tetragonon lived in a pebbly band along one edge of the beach, by a quay. Their feeding rate was comparable in both sexes and slower than that of U. vocans; they fed largely on filamentous algae growing on the quay, which provides better food, and fed faster during flood tide than ebb tide. They spent more time in waving and other sex-related activities, and were seldom aggressive, except during the week of the full moon. Burrowing activities included placing excavated mud balls some distance away from their burrows and re-arranging them. U. dussumieri inhabited the other end of the beach in muddier substrate. They did not have sex differences in feeding rates and their rate of scooping food into their mouths was slow, but feeding claws made multiple pinches of the substrate, thus accumulating more material in each clawful of food.     

Variation in the Boldness of Courting Sand Fiddler Crabs (Uca pugilator)

Individuals can express boldness in their readiness to resume courtship signaling following a perceived threat. The degree of boldness that is selectively favored depends on the magnitude of costs and benefits that may vary across time and space. We examined within‐ and between‐individual variation in the boldness of courting male sand fiddler crabs, Uca pugilator, across an entire breeding season at a South Carolina (USA) salt marsh where courtship is restricted to supratidal embankments. Boldness was assessed by the time to re‐emergence and the number of re‐emergences of males who were purposely startled into their breeding burrows once every 3 min for a total of five times. The two measures of boldness were significantly positively correlated. Courting males are on average bolder when their density is high and when tidal conditions correspond to peaks in the number of females moving over the embankment surface. Time to re‐emergence increases with successive startles although some males consistently re‐emerge faster than others. Large males are not bolder than small males. When male density is high, nearest neighbors frequently re‐emerge at the same time, suggesting that males cue on the responses of other nearby males, perhaps by assessing substrate vibration. This may reduce the chance of losing a potential mate to a local competitor.     

Waving Display in Females of Uca polita and of other Australian Fiddler Crabs

Since 1979 it is known that, in Australian species of Uca, female waving exists in addition to usual male display. The present paper deals mainly with female waving in U. polita studied in Darwin (North Australia). A few remarks on U. dampieri, U. vomeris, U. seismella and U. hirsutimanus are added. The species mentioned are members of two species groups or subgenera, which characterizes female waving as an ancestral (plesiomorph) trait. Frame by frame analysis of film sequences (open air shots) indicate homology of movements in the two sexes of U. polita. As in males, waving of females can be combined with locomotion on radial paths starting from the burrow entrance and the display is performed in series with a corresponding number of gestures. Unlike males, waving females mostly use both their chelipeds and tend to show shorter durations with regard to many of the waving parameters chosen. However, significant differences refer only to a limited number of parameters. The biological context of female waving was gathered from films and field observations. High intensity waving is released by conspecifics approaching from far (wanderers without burrows) and from the neighbourhood. Typically, only females and small males elicit high intensity display in a resident female. Waving normally stops in presence of larger males, especially of the male living in a resident breeding unit with the female in question. In spite of this, a pure agonistic (defensive) character of female waving is unlikely. Advertising of breeding condition seems to play a role similar to that in males. The few displaying females that exist in a given colony (about 2.5% in U. polita) show signs of special sexual excitement: brightening of carapace colours and sometimes spontaneous performance of waving, i.e. display immediately after emergence from the burrow in absence of any conspecific.     

Display Specificity and Reproductive Isolation in the Fiddler Crabs,Uca panacea and U. pugilator

The factors responsible for reproductive isolation between two sibling species of fiddler crabs (Uca pugilator and U. panacea) were studied under both laboratory and field conditions. ♂♂ showed species differences in their visual and acoustical displays. These differences were exaggerated in the overlap zone, where U. pugilator showed character displacement of its acoustic signals. ♀♀ of U. pugilator confined with ♂♂ of U. panacea produced fewer clutches of young. Occasionally, forced matings took place in the laboratory, resulting in hybrids suffering greater mortality through development. The data indicate that both premating (behavioral) as well as postmating (higher larval mortality) barriers act to prevent interbreeding.     

A Mathematical Modelling for the Cheliped Regeneration with Handedness in Fiddler Crab

An enormously developed giant cheliped with the other small one characterizes the adult male fiddler crab. Some experiments with artificial severances of cheliped indicate that such a handedness in the cheliped size is maintained even after the regeneration of severed cheliped. Other experimental researches give some results about an unknown physiological system which controls the emergence and the regeneration of the handedness in the cheliped size. In this paper, with two hypothesized factors relevant to the regeneration of a severed cheliped, we propose a simple mathematical model to describe the experimental result about the cheliped regeneration with a handedness after the cheliped severance for the fiddler crab. Our model gives a suggestion about an underlying system for the cheliped regeneration in the fiddler crab or some other crustacean species.