Evolutionary variation in the mechanics of fiddler crab claws
© Swanson et al.; licensee BioMed Central Ltd. 2013
Received: 5 October 2012
Accepted: 4 June 2013
Published: 15 July 2013
Fiddler crabs, genus Uca, are classic examples of how intense sexual selection can produce exaggerated male traits. Throughout the genus the enlarged “major” cheliped (claw) of the male fiddler crab is used both as a signal for attracting females and as a weapon for combat with other males. However, the morphology of the major claw is highly variable across the approximately 100 species within the genus. Here we address variation, scaling, and correlated evolution in the mechanics of the major claw by analyzing the morphology and mechanical properties of the claws of 21 species of fiddler crabs from the Pacific, Gulf and Atlantic coasts of the Americas.
We find that the mechanics that produce claw closing forces, the sizes of claws and the mechanical strength of the cuticle of claws are all highly variable across the genus. Most variables scale isometrically with body size across species but claw force production scales allometrically with body size. Using phylogenetically independent contrasts, we find that the force that a claw can potentially produce is positively correlated with the strength of the cuticle on the claw where forces are delivered in a fight. There is also a negative correlation between the force that a claw can potentially produce and the size of the claw corrected for the mass of the claw.
These relationships suggest that there has been correlated evolution between force production and armoring, and that there is a tradeoff between claw mechanics for signaling and claw mechanics for fighting.
The evolution of exaggerated male secondary sex characteristics is frequently attributed to sexual selection either by female choice or combat among males [1, 2]. To differentiate these two modes of selection, traits are separated into two groups based on their morphology and function. Morphological characters that are enlarged, conspicuously colored or shaped (e.g. peacock rump feathers), and are used primarily during courtship are ornaments; they are selected by female preferences that govern mate choice [3, 4]. Morphological characters that are used as weapons are armaments; they are selected for their utility in intra-sexual combat [2, 5].
Like many sexual ornaments, the major claw grows with positive allometry [12, 13]. It is made conspicuous as an ornament by its coloration, reflectance , shape , and size . Males of most species use their major claw in a variety of complex claw-waving displays that differ greatly across species [17–19]. Females have been shown to choose mates based on a complex set of species-specific criteria, which include, body or claw size [9, 20–22], wave rate or height [17, 23–25], burrow residency, and burrow quality [20, 26–28]. Waves not only attract females to a male’s burrow for mating, but also ward off ‘wandering’ males that fight burrow residents for their burrows [8, 18, 29, 30]. It is also possible that females select costly displays (vigorous waving with heavy claws) as a measure of male quality , however females will still select cheating males with regenerated claws and little combat ability . The importance of the waving display led Huxley  to conclude that the major claw evolved primarily for signaling, with combat as an incidental secondary use, made possible by the increase in claw size.
However, it is important to note that the claws of all fiddler crab species that have been studied must effectively perform both of these functions. For instance, an individual with purely signaling morphology would be at an energetic advantage in both development and display, but would not be able to defend territory and should have low fitness . Alternatively, a crab with a shorter or excessively heavy claw, although successful in gaining and defending territory, would incur an energetic cost and may not be able to attract females, therefore having lower fitness [17, 23–25]. Here we examine how a diverse set of fiddler crabs solve the problem of conflicting sexual selection on claw morphology. First, we examine variation across the clade and allometry of the mechanics of the claw across species. Second, we examine the relationship between claw mechanics and the mechanical properties of the cuticle. Third, we ask whether there is evidence of a tradeoff between mechanics that should maximize the claw’s effectiveness as a sexual signal and mechanics that should maximize the claw’s effectiveness as a weapon.
We found that the mechanics of the major claw are highly variable across species. This has been observed by others [8–10] and it is known that claw strength is tightly, positively correlated with size . However, even when the effect of size is removed we found variation of more than two-fold in claw force potential across species (Figure 3). This is due to variation in apodeme area (a proxy for muscle physiological cross sectional area) and morphology of the dactyl (Figure 2).
We also found that the force required to fracture the cuticle of the claw is variable, even with the effect of size removed (Figure 3). This variation probably results from differences in the material properties, thickness and shape of the cuticle. For instance, crabs may produce resistant claws by either making their cuticular material stronger or by producing a thicker cuticle. We do not know how the material properties vary across species, and this will be a focus of future work. We do know that body size corrected claw mass is correlated with resistance to puncture, suggesting that crabs increase resistance by increasing cuticle thickness (not shown).
Although mechanical properties of the claw are correlated with body size, there is precedent to suggest that sexually selected traits should scale allometrically [12, 13, 32]. However, Bounduriansky  suggests that this purported pattern is due to sampling bias and argues that under varying selective circumstances there should be different allometric patterns. We find no evidence that simple measurements of claw size are positively allometric across species (Figure 4). This contrasts with pronounced positive developmental allometry within some species of Uca[12, 13], and suggests that there may be different patterns of selection acting on different species . Most of the variation in claw mechanics across species seems to be associated with isometric scaling. The only exception is claw force production, which may suggest that this trait is under intense sexual selection across the clade. Alternatively, claw size, but not force, may be constrained. Levinton and Judge  noted that claw length seems to be constrained by carapace width so that claws do not extend beyond the contralateral edge of the carapace. When the crab rotates to enter its burrow the tip of the claw must go with the body (males hold their claws “folded” across their front when they enter their burrow). Hence, claw length at full adult size would scale isometrically with body width across species. The forces a claw can produce do not seem to be under this constraint.
Claw force and cuticle strength
When we compare the average force produced by the claws of a species to the resistance of the cuticle of that species to puncture, we find that all species should be able to break the carapace but not the manus of conspecifics with their claw tips (Figure 5). This makes sense in light of the ritualized combat seen in fiddler crabs, where only the manus (and not the carapace, which would cause serious injury) is gripped during aggressive interactions [8–10]. Like other species of crabs, male fiddler crabs grip each other’s major claw manus with the tubercles within the gape of their own major claw. The mechanical advantage at the tubercles within the gape of fiddler crab claws exceeds that at the tip of the claw. This seems to result frequently in surface indents, or small cuticular failures at the point where the tubercles contact the manus . We found that the forces at these tubercles and the forces required to cause an indentation in the cuticle of the manus of the claw were very similar across all species (Figure 5). This may reflect an optimization between force production and cuticular strength where the forces are received in a fight. We assume that increasing either of these variables comes at a cost. In fact, Murai et al.  found that experimentally increasing the mass of the claw not only increases the waving cost, but also decreases the wave height, an important component of female choice. It appears that crabs produce cuticles just strong enough to resist damage from most of their conspecifics, and have claws strong enough to cause slight surface damage to opponent’s claws. This provides a mechanical explanation for why males usually choose to fight males their size or slightly smaller , and why larger crabs tend to win . This could also help explain why crabs with regenerated and presumably weaker claws lose in fights .
As expected, larger crab species produce more force and are more resistant to cuticular damage. However, when the effects of size and phylogenetic relatedness are removed, there is still a significant positive relationship between force production and resistance to puncture (Figure 6). Hence, species with especially powerful claws also tend have especially armored claws, suggesting that these traits have evolved in concert. It also suggests that selection on claw force or cuticle resistance varies across the Uca clade.
A possible tradeoff between signaling and force
One of the most intriguing features of the major claw is that it functions both as a semaphore and a weapon. The mechanical properties one expects of semaphores or signaling flags are very different from those one expects of weapons. We suggest that flags (visual signals) should be large and lightweight to minimize the cost of display. It has been shown that claw size, and especially length, are selected by females . However, it has also been shown that male fiddler crabs incur significant energetic costs displaying with their massive claw . Weapons, on the other hand, should be relatively short to maximize mechanical advantage and heavy to maximize cuticle thickness and muscle cross sectional area . Indeed, we found an inverse relationship between claw force production and both the frontal area of the claw divided by claw mass and the length of the claw divided by claw mass (with the effects of body size and phylogenetic relatedness removed; Figure 7). There are of course alternative explanations for this pattern. For instance, both of these variables may be driven by some unmeasured variable. We also do not know the actual energetic costs of waving in any of the species studied here. There are also compensation mechanisms that allow species to have large displays and strong claws. For instance, U. terpsichores has an above average claw force and an above average mass specific claw area (Figure 3) . However, in general we expect that species in which combat is more important in determining male success should have claws that mechanically are more like weapons, and that species in which signaling is more important should have claws that are mechanically more like flags. For instance, U. heteropleura and U. saltitanta both have claws that are mechanically weak and seem to have exceptionally intense waving behaviors [; personal observations].
Within the more derived clades of fiddler crabs, we see several examples of the evolution of more forceful claws that can produce and resist much higher forces than the basal clade. However, this seems to come at a cost in that these claws are relatively smaller and are heavier. We hypothesize that these changes in claw structure are likely due to changes in social structure or courtship behavior. However, this remains to be tested experimentally. There are several examples where strong or resistant claws are found on species where the importance of waving seems to be reduced. For instance, U. argillicola is a small species with an unusually powerful claw that has never been observed to wave. U. leptodactyla has strong and resistant claws that seem to be waved infrequently. U. stenodactylus has a resistant claw and seems to have a mating system where female choice has reduced importance [9; personal observations]. With selection for signal function relaxed, incidental use of these claws for defense against predators might further accentuate mechanical features that make them good weapons. Unfortunately, the details of mate choice and aggressive interactions have not been well-studied in most Uca species. We suggest that our results should lead to more detailed examinations of these behaviors to see if our predictions hold. Hunt et al.  suggest that when selective forces act in opposition, variation in the timing, strength and direction of selection can produce a range of possible outcomes. This seems to be the case with fiddler crabs, where different morphologies may have been produced by variations in the details of the selective regime in each species.
Fiddler crabs are one of the classic examples of female choice producing an exaggerated, male trait, the major claw [9, 12]. However, our analysis suggests that the evolution of the major claw has been much more complex and interesting than if it had been selected only for signaling. The evolutionary challenge for a fiddler crab is to produce a conspicuous semaphore that retains its utility as a formidable weapon (the problem of how to design a “beautiful weapon”; ). There is significant variation in the mechanics of claws across species, both in force production and armoring. Within this variation, we find evidence of an evolutionary tradeoff, where different species solve this central problem of conflicting selection in different ways. Conflicting selection may maintain genetic and morphological diversity in species , and we suggest that it may also drive the evolution of morphological and functional diversity within a clade.
(A) sample collection and morphological measurements
List of species sampled and collection sites for the crabs used in this study
Diablo Heights, Panama
1.04 ± 0.59
12.62 ± 2.44
7.35 ± 0.68
0.64 ± 0.11
0.14 ± 0.03
0.41 ± 0.09
9.03 ± 0.74
Diablo Heights, Panama
0.54 ± 0.2
Diablo Heights, Panama
1.89 ± 0.66
16.14 ± 1.89
2.28 ± 1.01
0.39 ± 0.2
17.64 ± 2.28
0.26 ± 0.08
0.05 ± 0.02
7.37 ± 0.70
3.35 ± 0.61
0.58 ± 0.16
20.09 ± 1.28
0.34 ± 0.09
0.08 ± 0.03
8.76 ± 0.70
1.50 ± 0.84
1.17 ± 0.30
0.17 ± 0.06
12.46 ± 1.00
2.45 ± 0.63
0.67 ± 0.25
16.82 ± 1.44
Panacea, Florida, USA
1.55 ± 0.45
0.26 ± 0.09
14.84 ± 1.43
0.32 ± 0.15
14.67 ± 1.46
0.39 ± 0.07
0.09 ± 0.02
8.08 ± 0.54
0.88 ± 0.15
0.19 ± 0.04
11.65 ± 0.60
8.38 ± 2.77
1.48 ± 0.62
26.04 ± 2.97
0.49 ± 0.07
0.08 ± 0.02
9.93 ± 0.54
Diablo Heights, Panama
3.95 ± 1.83
0.74 ± 0.47
19.38 ± 3.02
Panacea, Florida, USA
0.91 ± 0.62
0.12 ± 0.14
12.46 ± 2.50
Individuals were removed from their burrows and measurements were taken in the field. Carapace breadth (mm) was measured with digital calipers (Mitutoyo, CD-6”CSX). Total mass of each individual (g) was determined with a digital scale (Ohaus, Scout Pro). For each individual, pressure was applied to both the anterior and posterior surfaces of the merus, resulting in the autonomy of the major cheliped. We immediately released these males close to where they were collected. The mass of the major claw was recorded (g) without the carpus or merus attached. Removed limbs were placed in labeled plastic bags filled with seawater and transported on ice to the Smithsonian Tropical Research Institution’s Naos Laboratory, Panama. Five whole individuals of each species were also collected for carapace analysis. The averages with standard deviations for carapace breadth, total weight, and major claw weight of each species collected are presented in Table 1.
All samples were analyzed within 10 hours of collection. A photo was taken of each major claw with a Pentax Optio W60 camera. Major claw length was the distance from the base of the juncture between carpus and manus and the tip of the pollex. The dactyl height (in-lever length) was measured from the fulcrum to the insertion of the closer apodeme (Figure 2: . Dactyl length (out-lever length) was split into two measurements due to variation of claw morphologies across species. The distance from the fulcrum to the dactyl tip and to the innermost large tubercle was recorded (Figure 2). All measurements were taken using ImageJ (http://rsbweb.nih.gov/ij/).
(b) resistance to puncture
Within the genus Uca, intra-specific fighting between males can escalate into high intensity combat where two individual’s major claws interlock while each crab grips the other . In this position, tubercles on the dactyl come into contact with the anterior manus of the opponent . In light of this behavior, we designed a macro-scale puncture test to measure how the manus of the major claw reacts to point forces. Using an INSTRON Inspec 2200 portable bench-top materials tester (INSTRON, Norwood, MA, USA), the anterior surface of the manus, where claw-closing forces are delivered, was punctured using a conical tip that emulated the shape of the tubercles. This produced a force/displacement curve. The first peak of each curve was interpreted as the force at which the cuticle of the major claw began to fail. This caused a small, circular indentation in the cuticle, like those often seen on the claws of crabs in the field [10, personal observation]. The tip was advanced further and force increased until the manus cuticle structurally failed (cracked) and force dropped. This procedure was repeated on three locations on the carapace (dorsal surface) of a subset of five individuals per species.
(c) estimation of closing force
We used morphological measurements to estimate the closing force of the major claw. Crabs have a bipinnate closer muscle in the manus of each claw that is attached to a chitinous disk, the closer apodeme (Figure 2; ). Contraction of the closer muscle pulls on this apodeme from both sides. The apodeme is connected to the base of the dactyl and closer muscle contraction produces a moment (force of the muscle*height of the dactyl, Figure 2) and rotates the dactyl [11, 37, 38]. Force is then exerted at the tip of the claw or the tubercles within the gape of the claw. Closing force is therefore a function of the stress produced per cross-sectional area of muscle, the cross-sectional area of the closer muscle (MCA, which is equal to 2* apodeme area) [37, 38] and the mechanical advantage of the lever arm (MA, which is the ratio of the dactyl height (the “in lever,” measured from fulcrum to the point of connection with apodeme) to the length of the lever arm (the “out lever,” measured from the fulcrum to the point force is applied); Figure 2; [39–41].
Two MA values were defined when appropriate, one using the out-lever length to the tip of the claw and the other to the most proximal tubercle in the gape of the claw. Apodeme area was determined by photographing the exposed apodeme and measuring its area using ImageJ (http://rsbweb.nih.gov/ij/).
(d) statistical analysis
When comparing morphological characters among species, the relative size and the phylogenetic history of each species can drive correlations [42, 43]. To correct for differences in size, we took the ln of the mean of each morphological character of each species and plotted that value against the ln of the mean of the body mass of each species. Residuals of the OLS regression were calculated giving values of each morphological measurement that were corrected for mass and normalized for each species . Phylogenetically independent contrasts of the species values (mass corrected and normalized) of each morphological measurement were determined using the PDAP package for Mesquite [45, 46] and the strict consensus of 8 most-parsimonious trees of the genus from Rosenburg . A series of different branch lengths were tried in the analysis. Setting all branch lengths equal to one minimized the relationship between the absolute values of the standardized independent contrasts and their standard deviations . We therefore set all branch lengths equal to one when calculating phylogenetically independent contrasts for subsequent analysis. When there is no phylogenetic signal in the data, non-phylogenetically corrected statistics are more appropriate. However, univariant estimates of phylogenetic signal can fail to detect it in some situations . Therefore, correlations between variables were also explored without phylogenetic correction.
We estimated the efficiency of the major claw as a signal two ways 1) as the ratio of the length of the claw to the mass of the claw, and 2) as the ratio of the surface area of the claw (its visually apparent size) to the mass of this structure. Large values of these ratios indicate a large claw of small mass that should require relatively little energy to wave.
This work was supported by the Gonzaga University office of sponsored research, the M.J. Murdock charitable trust, HHMI and the AFOSR (grant FA9550-10-1-0209 to BOS). Alexei Maklakov and two anonymous reviewers provided comments on earlier versions of the manuscript. We also thank the staff of the STRI for logistical support.
- Darwin C: The descent of man and selection in relation to sex. 1871, London: MurrayView ArticleGoogle Scholar
- Berglund A, Bisazza A, Pilastro A: Armaments and ornaments: an evolutionary explanation of traits of dual utility. Biol J Linn Soc. 1996, 58 (4): 385-399. 10.1111/j.1095-8312.1996.tb01442.x.View ArticleGoogle Scholar
- Fisher RA: The evolution of sexual preference. Eugen Rev. 1915, 7: 184-192.PubMed CentralPubMedGoogle Scholar
- Andersson M: Sexual Selection. 1994, Princeton, NJ: Princeton Univ Press, 599-Google Scholar
- Emlen D: The evolution of Animal Weapons. Annu Rev Ecol Evol Syst. 2008, 39: 387-413. 10.1146/annurev.ecolsys.39.110707.173502.View ArticleGoogle Scholar
- Hunt J, Breuker CJ, Sadowski JA, Moore AJ: Male-male competition, female mate choice and their interaction: determining total sexual selection. J Evol Biol. 2008, 22: 13-26.View ArticleGoogle Scholar
- Candolin U: Opposing selection on a sexually dimorphic trait through female choice and male competition in a water boatman. Evolution. 2004, 58: 1861-1864.PubMedView ArticleGoogle Scholar
- Crane J: Combat, display and ritualization in fiddler crabs (ocypodidae, genus Uca). Philos Trans R Soc Lond B Biol Sci. 1966, 251: 459-72. 10.1098/rstb.1966.0035.View ArticleGoogle Scholar
- Crane J: Fiddler Crabs of the World: OCYPODDAE: GENUS UCA. 1975, Princeton, NJ: Princeton University Press,Google Scholar
- Dennenmoser S, Christy J: The design of a beautiful weapon: compensation for opposing sexual selection on a trait with two functions. Evolution. 67 (4): 1181-1188.Google Scholar
- Levinton JS, Allen BJ: The paradox of the weakening combatant: trade-off between closing force and gripping speed in a sexually selected combat structure. Funct Ecol. 2005, 19 (1): 159-65. 10.1111/j.0269-8463.2005.00968.x.View ArticleGoogle Scholar
- Huxley JS: Problems of relative growth. 1932, New York: Lincoln Mac Veagh—The Dial PressGoogle Scholar
- Levinton JS, Judge ML: The relationship of closing force to body size for the major claw of Uca pugnax (decapoda: Ocypodidae). Funct Ecol. 1993, 7 (3): 339-45. 10.2307/2390214.View ArticleGoogle Scholar
- Cummings ME, Jordão JM, Cronin TW, Oliveira RF: Visual ecology of the fiddler crab, uca tangeri: Effects of sex, viewer and background on conspicuousness. Anim Behav. 2008, 75 (1): 175-88. 10.1016/j.anbehav.2007.04.016.View ArticleGoogle Scholar
- Takeda S, Murai M: Asymmetry in male fiddler crabs is related to the basic pattern of claw-waving display. Biol Bull. 1993, 184 (2): 203-8. 10.2307/1542227.View ArticleGoogle Scholar
- Backwell PRY, Christy JH, Telford SR, Jennions MD, Passmore J: Dishonest signalling in a fiddler crab. Proc R Soc Lond B Biol Sci. 2000, 267 (1444): 719-24. 10.1098/rspb.2000.1062.View ArticleGoogle Scholar
- Crane J: Basic patterns of display in fiddler crabs (ocypodidae, genus Uca). Zoologica. 1957, 42: 69-82.Google Scholar
- Pope DS: Waving in a crowd: fiddler crabs signal in networks. Animal Communication Networks. Edited by: McGregor PK. 2005, Cambridge: Cambridge University PressGoogle Scholar
- How MJ, Zeil J, Hemmi JM: Variability of a dynamic visual signal: the fiddler crab claw-waving display. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2009, 195 (1): 55-67. 10.1007/s00359-008-0382-7.PubMedView ArticleGoogle Scholar
- Reaney LT, Backwell PRY: Temporal constraints and female preference for burrow width in the fiddler crab, Uca mjoebergi. Behav Ecol Sociobiol. 2007, 61: 1515-1521. 10.1007/s00265-007-0383-5.View ArticleGoogle Scholar
- Milner RNC, Detto T, Jennions MD, Backwell PRY: Experimental evidence for a seasonal shift in the strength of a female mating preference. Behavioural Ecology. 2010, 21: 311-316. 10.1093/beheco/arp196.View ArticleGoogle Scholar
- Jaroensutasinee M, Jaroensutasinee K: Male body size influences female choice and male-male competition in the fiddler crab, Uca paradussumieri Bott, 1973 (Decapoda, Brachyura, Ocypodidae). Crustaceana. 2003, 76: 177-186. 10.1163/156854003321824521.View ArticleGoogle Scholar
- Murai M, Backwell PRY: A conspicuous courtship signal in a fiddler crab Uca perplexa: female choice based on display structure. Behav Ecol Sociobiol. 2006, 60: 736-741. 10.1007/s00265-006-0217-x.View ArticleGoogle Scholar
- Murai M, Backwell PRY, Jennions MD: The cost of reliable signaling: experimental evidence for a predictable variation among males in a cost-benefit trade-off between sexually selected traits. Evolution. 2009, 63 (9): 2363-2371. 10.1111/j.1558-5646.2009.00726.x.PubMedView ArticleGoogle Scholar
- Callander C, Jennions MD, Backwell PRY: The effect of claw size and wave rate on female choice in a fiddler crab. J Ethol. 2012, 30: 151-155. 10.1007/s10164-011-0309-6.View ArticleGoogle Scholar
- Christy JH: Female choice and the breeding behavior of the fiddler crab Uca beebei. J Crust Biol. 1987, 7 (4): 624-35.View ArticleGoogle Scholar
- Christy JH: Burrow structure and use in the sand fiddler crab, Uca pugilator (Bosc). Anim Behav. 1982, 30: 487-494.View ArticleGoogle Scholar
- de Rivera CE: Long searches for male-defended breeding burrows allow female fiddler crabs, Uca crenulata, to release larvae on time. Anim Behav. 2005, 70: 289-297. 10.1016/j.anbehav.2004.10.027.View ArticleGoogle Scholar
- Christy JH: Female choice in the resource-defense mating system of the sand fiddler crab, uca pugilator. Behav Ecol Sociobiol. 1983, 12 (2): 169-80. 10.1007/BF00343209.View ArticleGoogle Scholar
- Hyatt GW, Salmon M: Combat in the fiddler crabs Uca pugilator and U. pugnax: a quantitative analysis. Behaviour. 1978, 65 (3/4): 182-211.View ArticleGoogle Scholar
- Jennions MD, Backwell PRY: Residency and size affect fight duration and outcome in the fiddler crab Uca annulipes. Biol J Linn Soc. 1996, 57 (4): 293-306.Google Scholar
- Gould SJ: Positive allometry of antlers in the Irish elk, Megaloceros giganteus. Nature. 1973, 244: 375-376. 10.1038/244375a0.View ArticleGoogle Scholar
- Bonduriansky R: Sexual selection and allometry: a critical reappraisal of the evidence and ideas. Evolution. 2007, 61: 838-849. 10.1111/j.1558-5646.2007.00081.x.PubMedView ArticleGoogle Scholar
- Murai M, Backwell PRY, Jennions MD: Experimental evidence for predictable variation among males in a cost-benefit trade-off between sexually selected traits. Evolution. 2009, 63: 2363-2371. 10.1111/j.1558-5646.2009.00726.x.PubMedView ArticleGoogle Scholar
- Morrell LJ, Backwell PRY, Metcalfe NB: Fighting in fiddler crabs Uca mjoebergi: what determines duration?. Anim Behav. 2005, 70: 653-662. 10.1016/j.anbehav.2004.11.014.View ArticleGoogle Scholar
- Matsumasa M, Murai M: Changes in blood glucose and lactate levels of male fiddler crabs: effects of aggression and claw waving. Anim Behav. 2005, 69: 569-577. 10.1016/j.anbehav.2004.06.017.View ArticleGoogle Scholar
- Warner GF, Jones AR: Leverage and muscle type in crab chelae (crustacea: Brachyura). J Zool. 1976, 180: 57-68.View ArticleGoogle Scholar
- Schenk SC, Wainwright PC: Dimorphism and the functional basis of claw strength in six brachyuran crabs. J Zool. 2001, 255 (01): 105-10.1017/S0952836901001157.View ArticleGoogle Scholar
- Vermeij GJ: Patterns in crab claw size: The geography of crushing. Syst Zool. 1977, 26 (2): 138-51. 10.2307/2412837.View ArticleGoogle Scholar
- Elner RW: The mechanics of predation by the shore crab, carcinus maenas (L.), on the edible mussel. Mytilus edulis (L.) Oecologia. 1978, 36 (3): 333-44. 10.1007/BF00348059.View ArticleGoogle Scholar
- Elner RW, Campbell A: Force, function and mechanical advantage in the chelae of the american lobster homarus americanus (decapoda: Crustacea). J Zool, Lond. 1981, 193-269.Google Scholar
- Kermack KA, Haldane JBS: Organic correlation and allometry. Biometrika. 1950, 37: 30-41.PubMedView ArticleGoogle Scholar
- Garland T, Harvey PH, Ives AR: Procedures for the analysis of comparative data using phylogenetically independent contrasts. Syst Biol. 1992, 41: 18-32.View ArticleGoogle Scholar
- Riggs DS, Guarnieri JA, Addelman S: Fitting straight lines when both variables are subject to error. Life Sci. 1978, 22: 1305-1360. 10.1016/0024-3205(78)90098-X.PubMedView ArticleGoogle Scholar
- Maddison WP, Maddison DR: Mesquite: a modular system for evolutionary analysis. 2009, Version 2.72, 2009. [http://mesquiteproject.org]Google Scholar
- Midford PE, Garland T, Maddison W: PDAP:PDTREE package for Mesquite. 2008, Version 1.12. 2008. [http://mesquiteproject.org/pdap_mesquite/]Google Scholar
- Rosenberg MS: The systematics and taxonomy of fiddler crabs: a phylogeny of the genus Uca. J Crust Biol. 2001, 21 (3): 839-69. 10.1651/0278-0372(2001)021[0839:TSATOF]2.0.CO;2.View ArticleGoogle Scholar
- Revell LJ: Phylogenetic signal and linear regression on species data. Methods in Ecology and Evolution. 2010, 1: 319-329. 10.1111/j.2041-210X.2010.00044.x.View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.