Intraspecific trait cospecialization of constitutive and inducible morphological defences in a marine snail from habitats with different predation risk

1.?Studies examining the integration of constitutive and inducible aspects of multivariate defensive phenotypes are rare. 2.?I asked whether marine snails (Nucella lamellosa) from habitats with and without abundant predatory crabs differed in constitutive and inducible aspects of defensive shell morphology. 3.?I examined multivariate shell shape development of snails from each habitat in the presence and absence of waterborne cues from feeding crabs (Cancer productus). I also examined the influence of constitutive and inducible shell morphology on resistance to crushing. 4.?Regardless of the presence of crabs, snails from high-risk (HR) habitats developed rotund, short-spired shells, while snails from low-risk habitats developed elongate shells, tall-spired shells, indicating among-habitat divergence in constitutive shell shape. Moreover, allometry analyses indicated that constitutive developmental patterns underlying this variation also differed between habitats. However, snails from HR habitats showed greater plasticity for apertural lip thickness and apertural area in the presence of crab cues, indicating among-habitat variation in defence inducibility. 5.?Both shell shape and apertural lip thickness contributed to shell strength suggesting that constitutive shell shape development and inducible lip thickening have evolved jointly to form an effective defence in habitats where predation risk is high.     

The effects of exposure and predation on the shell of two British winkles

Changes in shell size and shell shape of the two British winkles Littorina nigrolineata and L. rudis were studied in relation to exposure and to crab-size. In both species, shells from exposed shores are smaller and more globose than those from sheltered shores. Also, in rudis of exposed shores the mouth is relatively wider. In shores of equally sheltered conditions, shells are bigger at those localities where crabs are large than at those localities where they are small. The largest shells are found in those localities where it is extremely sheltered, and the crabs are very large.
It is argued that on exposed shores, small shells are favoured because they have more possibilities than large ones to shelter in crevices and in barnacle interspaces, from the impact of winds and waves. A globose shell could accommodate more foot muscle and thus enable a stronger adherence to the rock; and an increased mouth diameter would increase the area of foot adherence to the rock. On sheltered shores, on the other hand, large, narrow-mouthed shells are favoured because they discourage crab predation, large crabs being abundant mainly on sheltered shores.
The possible significance of shell size and shape in relation to zonation is discussed, in view of the different predatory and physical conditions which prevail in different zones of the shore, and the different shell specializations which these conditions would require.     

Plastic and heritable components of phenotypic variation in Nucella lapillus: an assessment using reciprocal transplant and common garden experiments

Assessment of plastic and heritable components of phenotypic variation is crucial for understanding the evolution of adaptive character traits in heterogeneous environments. We assessed the above in relation to adaptive shell morphology of the rocky intertidal snail Nucella lapillus by reciprocal transplantation of snails between two shores differing in wave action and rearing snails of the same provenance in a common garden. Results were compared with those reported for similar experiments conducted elsewhere. Microsatellite variation indicated limited gene flow between the populations. Intrinsic growth rate was greater in exposed-site than sheltered-site snails, but the reverse was true of absolute growth rate, suggesting heritable compensation for reduced foraging opportunity at the exposed site. Shell morphology of reciprocal transplants partially converged through plasticity toward that of native snails. Shell morphology of F(2)s in the common garden partially retained characteristics of the P-generation, suggesting genetic control. A maternal effect was revealed by greater resemblance of F(1)s than F(2)s to the P-generation. The observed synergistic effects of plastic, maternal and genetic control of shell-shape may be expected to maximise fitness when environmental characteristics become unpredictable through dispersal.     

Ontogeny of shell morphology and shell strength of the marine snails Littorina obtusata and Littorina mariae: different defence strategies in a pair of sympatric, sibling species

The sibling marine snails Littorina obtusata (L.) and Littorina mariae Sacchi & Rastelli are sympatrically distributed and the shells of both species are subject to similar breaking forces by predatory crabs. Nevertheless, the two species exhibit rather different growth and defence strategies. To determine growth patterns, we measured changes in five morphological variables with increasing shell length: body whorl thickness at the point of crushing force application, shell height (related to globosity), shell mass, body mass, and apertural lip thickness. We also measured ontogenetic changes in the ability to withstand shell crushing. For most morphological variables, L. mariae showed uniformly allometric growth of juveniles into adults. In contrast, L. obtusata usually exhibited a distinct change in growth pattern upon reaching maturity. As adults, L. mariae showed a more sustained increase in overall shell mass and in body whorl thickness (defence against crushing attacks) and also had proportionally thicker apertural lips (defence against peeling attacks). Littorina obtusata , however, grew to a larger size and their shells could accommodate larger bodies at all sizes. Furthermore, the strength of L. obtusata shells increased faster than could be accounted for by either overall shell mass or thickness at the point of force application, suggesting strengthening by other means such as changes in shell microstructure or shape (other than globosity). These results illustrate the viability of two contrasting antipredator strategies, despite a highly similar phylogenetic history and selective regime.     

MORPHOLOGY AND BEHAVIOR OF CRABS AND GASTROPODS FROM LAKE TANGANYIKA,AFRICA: IMPLICATIONS FOR LACUSTRINE PREDATOR-PREY COEVOLUTION

The shells of most lacustrine gastropods are typically small, weakly calcified, and modestly ornamented to unornamented. Similarly, most lacustrine crabs are usually small detritivores with weak chelae. A number of invertebrate taxa in Lake Tanganyika, however, deviate from these generalities. This study explores a predator-prey coevolution model as an explanation for the large, heavily calcified, and ornate gastropods and the robust, durophagous crabs of Lake Tanganyika. The endemic thiarid and viviparid gastropods from Lake Tanganyika have significantly thicker shells and higher frequencies of terminal apertural lip thickening than closely related cosmopolitan taxa from outside the lake. Tanganyikan gastropods also display considerably higher incidence of shell repair, following nonlethal shell damage, than cosmopolitan taxa of the same families. There is a strong positive correlation between gastropod apertural lip thickness and shell repair frequency among all the gastropod species analyzed. The endemic Tanganyikan potamonautid crab Platytelphusa armata (a molluscivore) possesses larger, more robust crushing chelae than other African potamonautid or potamonid crabs. In contrast with the cosmopolitan African crabs, the Tanganyikan crabs display molariform, rather than serrate dentition on their crushing chelipeds. In shell-crushing experiments, the Tanganyikan gastropod shells were an order of magnitude stronger than typical lacustrine gastropod shells, many well within the range of tropical marine gastropod shell strengths. Predation experiments with the endemic gastropods Spekia, Neothauma, Lavigeria spp., Paramelania spp. and the crab Platytelphusa armata showed that increased size, apertural lip thickness or shell sculpture reduced the successful predation rate of P. armata. Crabs with large chelae have a greater ratio of successful: unsuccessful attacks than crabs with small chelae. Among cases of successful predation, crabs with large chelae employed predation methods that required less time and energy (such as crushing the shell in the cheliped) than the methods employed by crabs with small chelae (such as peeling the shell from the aperture or the spire). The morphological, shell-crushing, and aquarium experiment data, considered in concert, provide strong support for the idea that the endemic gastropods and crabs of Lake Tanganyika have coevolved over the past 7 million years.     

Associations between shell morphology and land crab predation in the land snail Cerion

1. The land crab Gecarcinus lateralis is a significant predator of the abundant Bahamian land snails of the genus Cerion . The crabs typically 'scissor' the cylindrical shells in half or break the lip and peel back the shell to reach the animal which withdraws two or three whorls into the shell. Scars on shells of live adults at 73 sites in the Bahamas and Florida Keys show that about 8% (range: 0–44%) of the snails have survived attacks of this type.
2. An artificial crab claw was used to investigate the compressive force required to break Cerion shells of different morphotypes. Defining shell strength as the ability to withstand compressive forces, 10 morphotypes were found that exhibited mean relative strengths of between 30 and 300 newtons. Feeding trials with one adult crab showed that snails whose shells could withstand compressive forces of > 95 N were safe from this individual predator.
3. Multiple linear regression analyses showed that both shell size (length and width) and shell wall thickness were the ultimate determinants of shell strength. Ribs strengthen the shell by contributing to wall thickness and also by increasing overall shell width. The thickened adult shell lip and collabral ribs provide effective protection from attack by peeling.     

An inducible morphological defence is a passive by-product of behaviour in a marine snail

Many organisms have evolved inducible defences in response to spatial and temporal variability in predation risk. These defences are assumed to incur large costs to prey; however, few studies have investigated the mechanisms and costs underlying these adaptive responses. I examined the proximate cause of predator-induced shell thickening in a marine snail (Nucella lamellosa) and tested whether induced thickening leads to an increase in structural strength. Results indicate that although predators (crabs) induce thicker shells, the response is a passive by-product of reduced feeding and somatic growth rather than an active physiological response to predation risk. Physical tests indicate that although the shells of predator-induced snails are significantly stronger, the increase in performance is no different than that of snails with limited access to food. Increased shell strength is attributable to an increase in the energetically inexpensive microstructural layer rather than to material property changes in the shell. This mechanism suggests that predator-induced shell defences may be neither energetically nor developmentally costly. Positive correlations between antipredator behaviour and morphological defences may explain commonly observed associations between growth reduction and defence production in other systems and could have implications for the evolutionary potential of these plastic traits.     

Water-borne cues from a shell-crushing predator induce a more massive shell in experimental populations of an intertidal snail

Inducible defenses are important in the life strategies of many taxa. In some species of marine gastropods, water-borne chemical cues from potential predators induce defensive changes in shell form and differences in growth rate. We examined such phenotypic plasticity in the direct-developing snail, Littorina subrotundata (Carpenter, 1864). Among experimental field populations of L. subrotundata exposed to differing intensities of predation by the purple shore crab, Hemigrapsus nudus (Dana, 1851), snails collected from predation-intense environments often had more massive shells than closely related snails from adjacent environments where predation was negligible. Snails collected from both environments were raised in tanks containing cages of H. nudus that were feeding on conspecific snails and compared to a control group raised in the absence of this stimulus. Most snails developed significantly more massive shells in the presence of the crabs suggesting that adaptive phenotypic plasticity may account for some of the variation we observed in the field. In one case, snails from a predation-intense environment did not exhibit a statistically significant amount of plasticity, but instead grew a more massive shell irrespective of the laboratory stimulus. We interpret this as evidence for a genetic difference in the plasticity of shell form among experimental populations, caused by intense selection by H. nudus. There was no statistical difference in the growth rates of snails among treatments.     

Character displacement, frequency-dependent selection, and divergence of shell colour in land snails Mandarina (Pulmonata)

Endemic land snails of the genus Mandarina of the oceanic Bonin Islands offer an exceptional example of habitat and character divergence among closely related species. In this study, microhabitat differences between sympatric ground-dwelling species were studied by distinguishing habitats on the basis of vegetation and types of litter. In all sites where two ground species coexisted, segregation occurred with each species showing preference for the microhabitat in which they were found. When they were in sympatry, one species was predominant in relatively wet and sheltered sites and the other in relatively dry and exposed sites. Although most species can live in both types of habitat, occupation by one species is inhibited by occupation by another. This suggests that competitive interaction between sympatric species caused segregation. Except for populations that have undergone interspecific hybridization, no examples were found of sympatric populations of two ground species sharing a similar shell colour. Species that were predominant in relatively wet and sheltered sites possessed shells with dark coloration and their colour patterns were mostly of one type. Species that were predominant in relatively dry and exposed sites possessed shells with bright coloration and their color patterns were polymorphic. Most populations from areas in which single species were distributed had shells with medium coloration. Microhabitat differentiation between sympatric species possibly caused diversification of shell colour, because bright shells are advantageous in sites where snails are largely exposed, and dark shells are advantageous in sites in where they are mostly sheltered from sunlight. In addition, frequency-dependent selection by predators hunting by sight may have operated to maintain colour polymorphism in the populations which are restricted to exposed habitats by competition with other sympatric species. This reveals the importance of interaction among closely related species as a cause of diversification in ecological and morphological traits.     

Evidence of a reproductive barrier between two forms of the marine periwinkle Littorina fabalis (Gastropoda)

Studies of allozyme variation may reveal unexpected patterns of genetic variation which challenge earlier conclusions of species delimitations based on morphological data. However, allozyme variation alone may not be sufficient to resolve this kind of problem. For example, populations of the marine intertidal snail Littorina fabalis (=Littorina mariae) from wave exposed parts end from protected parts of the same shores are distinguished by different alleles of arginine kinase (Ark) while indifferent, or very nearly so, in another 29 loci. Intermediate populations have large deficiencies of exposed/sheltered heterozygote classes of Ark and we have earlier suggested habitat-related selection in this locus as the explanation. In this study we estimated growth rate of individual snails of different Ark-genotypes in three different habitats (exposed, sheltered and intermediate). In all habitats the snails homozygous for alleles of ‘exposed’ type grew faster and matured at a larger size than did snails homozygous for alleles of ‘sheltered’ types. This relationship was indirectly confirmed in three additional sites of intermediate exposure where exposed AA-genotypes dominated among large (>8 mm) snails while the sheltered genotypes dominated among small (<5 mm) snails of truly sympatric samples. We furthermore found small differences in allele frequencies of two other loci (Pgi and Pgm-2) and in shell colour frequencies, comparing sympatric snails of exposed and sheltered Ark-homozygotes. Although we found no signs of habitat-related selection among snails of different Ark-genotype, or selection against heterozygotes, we cannot reject selection in Ark, as our experiments only covered one island, one season and grown-up snails. The coupling between allozyme and phenotypic characters in strictly sympatric samples of snails suggests the presence of two gene pools. Perhaps the large and small forms of L. fabalis represent very closely related cryptic taxa. However, introgression between them seems a possible explanation for the striking similarities in the vast majority of morphological and allozyme characters.     

Crushing behavior of tropical and temperate crabs

The Guamunian xanthids Carpilius maculatus (L.), C. convexus (Forskal), and Eriphia sebana (Shaw & Nodder), and the parthenopid Daldorfia horrida (L.), possess large master claws with molariform teeth than are used to crush the shells of hermit crabs and snails. These crabs typically sever the spire of their prey, or make a gash in the body whorl. They tend to employ sustained pressure on the prey shell, and, except for Eriphia, rarely attack the outer lip, so that the outer lip of the shell typically remains undamaged, except in shells near the critical size, i.e., the maximum size of vulnerability to predation. Temperate species of Cancer (C. productus Randall and C. oregonensi Rathbun) may also crush shelled prey in the larger of their two claws, but more commonly they use both claws together in breaking open their victims. Sustained pressure is applied for only short periods by these crabs.Gastropod adaptations conferring resistance to crushing by crabs include a thick shell, narrow or otherwise small aperture, thickened outer lip, strong sculpture, and a low spire. Emphasis on these traits lowers the critical size of the prey, i.e., permits escape from cushing at a smaller size. An equatorward increase in the expression of the characteristics of crushing-resistance parallels an increase in crushing power of the crabs.     

Prey-induced changes to a predator's behaviour and morphology: Implications for shell-claw covariance in the northwest Atlantic

Whereas many plasticity studies demonstrate the importance of inducible defences among prey, far fewer investigate the potential role of inducible offences among predators. Here we ask if natural differences in a snail's shell hardness can induce developmental changes to a predatory crab's claw size. To do this, we fed Littorina obtusata snails from either thick- or thin-shelled populations to captive European green crabs Carcinus maenas. The crabs' shell-breaking behaviour dominated among those fed thin-shelled snails, whereas crabs fed thick-shelled snails mostly winkled flesh through the shell opening without damaging the shell itself (a.k.a. aperture-probing behaviour). Significantly, the size of crab crusher claws grew in proportion to the frequency of shell-crushing behaviour and, for a same shell-crushing frequency, crabs fed thick-shelled snails grew larger crusher claws than those fed thin-shelled snails after two experimental moults. Diet and behaviour had no effect on the growth of the smaller cutter claws of same individuals, providing good evidence that allometric changes to crusher claws were indeed a result of differential use while feeding. Findings indicate that both predation habits and claw sizes are affected by green crabs' diet, supporting the hypothesis that prey-induced phenotypic plasticity contributes to earlier accounts of shell-claw covariance between this predator and its Littorina prey in the wild.     

Predator-induced defenses in a salt-marsh gastropod

Predator-induced defenses are among the most ecologically important forms of phenotypic plasticity. Although predation and induced defenses are well documented in rocky-intertidal systems, they have received less attention in soft-bottom communities. Shell-crushing predators are common in soft-bottom, vegetated habitats, which often exhibit substantial spatial heterogeneity in predation intensity. We examined variations in shell morphology of the salt-marsh periwinkle, Littoraria irrorata, among marsh microhabitats in the northern Gulf of Mexico that vary in their accessibility to predatory blue crabs, Callinectes sapidus. Littoraria from high-predation sites exhibited more extensively calcified apertural lips and narrower apertural openings relative to snails from low-predation sites. Thick apertural lips generally increased the handling time required by Callinectes to breach Littoraria shells in laboratory experiments, although the method of shell entry used by crabs was dependent on the crab:snail size ratio. Apertural-lip thickness was not related to past predation events in field-collected snails. Snails exposed to water treated with the effluent of Callinectes and crushed conspecifics produced significantly thicker apertural lips than controls, with a response time and morphological extent comparable to that of their rocky-shore counterparts. This study underscores the widespread occurrence of predator-induced plasticity in marine gastropods and emphasizes its role in soft-bottom, vegetated marine habitats, where shell-crushing predation can be as prevalent a selective force as in the rocky intertidal.     

Effects of habitat on growth and shape of contrasting phenotypes of Bembicium vittatum Philippi in the Houtman Abrolhos Islands,Western Australia

Translocation experiments were used to test the effect of habitat on growth and shape of three contrasting phenotypes of Bembicium vittatum: dwarf, highly domed snails from an usually dry tidal pond; large, moderately domed snails from a sheltered, regularly inundated pond; and relatively flat snails from a vertical, exposed shore. Snails from both ponds grew nearly twice as fast in the wet pond as in the dry pond, indicating a high degree of plasticity of growth. Associated with these changes in growth rates was convergence of shape. Under conditions of rapid growth, the dwarf snails became relatively flatter, and hence more similar to the native snails at that site. These results indicate that the dwarf phenotype is largely a plastic stunting in response to conditions of little submersion time. The snails from the exposed shore also grew faster in the sheltered, wet pond than at their native site. However, they not only retained their flat shape, but actually became flatter (and hence divergent from the pond snails) when grown in the pond. Thus, variation in shell shape was due to interactions between source population and a common plastic association of flatter growth profile with more rapid growth. Previous experiments had demonstrated high heritability of the flat phenotype, while the present results show that the expression of the genetically different types is affected substantially by the conditions of growth, and that phenotypic differences among populations may either overestimate or underestimate the underlying genetic differences. This unpredictability of the relationship between variation in shell form and its underlying genetic basis complicates interpretations of geographical variation or palaeontological sequences based on shell form.     

Habitat-specific size structure variations in periwinkle populations (<Emphasis Type="Italic">Littorina littorea)</Emphasis> caused by biotic factors

Shell size distribution patterns of marine gastropod populations may vary considerably across different environments. We investigated the size and density structure of genetically continuous periwinkle populations (Littorina littorea) on an exposed rocky and a sheltered sedimentary environment on two nearby islands in the south-eastern North Sea (German Bight). On the sedimentary shore, periwinkle density (917 ± 722 individuals m⁻²) was about three times higher than on the rocky shore (296 ± 168 individuals m⁻²). Mean (9.8 ± 3.9 mm) and maximum (22 mm) shell size of L. littorea on the sedimentary shore were smaller than on the rocky shore (21.5 ± 4.2 and 32 mm, respectively), where only few small snails were found. Additionally, periwinkle shells were thicker and stronger on the rocky than on the sedimentary shore. To ascertain mechanisms responsible for differences in population structures, we examined periwinkles in both environments for growth rate, predation pressure, infection with a shell boring polychaete (Polydora ciliata) and parasitic infestation by trematodes. A crosswise transplantation experiment revealed better growth conditions on the sedimentary than on the rocky shore. However, crab abundance and prevalence of parasites and P. ciliata in adult snails were higher on the sedimentary shore. Previous investigations showed that crabs prefer large periwinkles infested with P. ciliata. Thus, we suggest that parasites and shell boring P. ciliata in conjunction with an increased crab predation pressure are responsible for low abundances of large periwinkles on the sedimentary shore while high wave exposure may explain low densities of juvenile L. littorea on the rocky shore. We conclude that biotic factors may strongly contribute to observed differences in size structure of the L. littorea populations studied on rocky and sedimentary shores.     

Phenotypic clines, plasticity, and morphological trade-offs in an intertidal snail

Understanding the genetic and environmental bases of phenotypic variation and how they covary on local and broad geographic scales is an important goal of evolutionary ecology. Such information can shed light on how organisms adapt to different and changing environments and how life-history trade-offs arise. Surveys of phenotypic variation in 25 Littorina obtusata populations across an approximately 400-km latitudinal gradient in the Gulf of Maine revealed pronounced clines. The shells of snails from northern habitats weighed less and were thinner and weaker in compression than those of conspecifics from southern habitats. In contrast, body size (as measured by soft tissue mass) followed an opposite pattern; northern snails weighed more than southern snails. A reciprocal transplant between a northern and southern habitat revealed substantial plasticity in shell form and body mass and their respective measures of growth. Southern snails transplanted to the northern habitat produced lighter, thinner shells and more body mass than controls raised in their native habitat. In contrast, northern snails transplanted to the southern site produced heavier, thicker shells and less body mass than controls raised in their native habitat. Patterns of final phenotypic variation for all traits were consistent with cogradient variation (i.e., a positive covariance between genetic and environmental influences). However, growth in shell traits followed a countergradient pattern (i.e., a negative covariance between genetic and environmental influences). Interestingly, body growth followed a cogradient pattern, which may reflect constraints imposed by cogradient variation in final shell size and thickness. This result suggests the existence of potential life-history trade-offs associated with increased shell production. Differences in L. obtusata shell form, body mass, and their respective measures of growth are likely induced by geographic differences in both water temperature and the abundance of an invading crab predator (Carcinus maenas). Water temperatures averaged 6.8 degrees C warmer during the transplant experiment and C. maenas abundance is greater in the southern Gulf of Maine. Because both increased water temperature and crab effluent affect shell form in the same way, future experiments are needed to determine the relative importance of each. Nevertheless, it is clear that phenotypic plasticity has an important role in producing geographic variation in L. obtusata shell form. Moreover, the evolution of phenotypic plasticity in L. obtusata and other marine gastropods may be driven by architectural constraints imposed by shell form on body mass and growth.     

Why small hermit crabs have large shells

Frequent shell exchanges among hermit crabs imply the enigmatic circumstance that large crabs frequently obtain large shells from smaller crabs. This seeming anomaly is explored as a key to the shell resource system. It is hypothesized to reflect how, where, and how often shells become available to the crabs. Shells become available infrequently, as snails die, and are available to the crabs for only a brief time before they become inaccessible. The standing crop of empty shells is almost always low and is irrelevant to rates of shell turnover in the crab population. Crabs are most likely to encounter shells of the wrong size, and the chance of encountering a shell of the desired size decreases as a crab grows. Snails and crabs are usually found on different portions of the shore; thus, crabs must make “foraging trips” for shells. Under this regime of shell supply, a crab will get a suitable shell the fastest when it accepts any fresh shell that is larger than its initial shell. It can then trade with other crabs to improve its shell fit. This behavior will make small crabs into a regular source of large shells for large crabs, and a shell exchange ritual will be strongly favored because both participants will benefit. Shells are an unusual resource because they are the object of both competitive and mutualistic interactions. This ambiguous quality is revealed in the intraspecific and interspecific responses of crabs to each other and to shells.     

Associations with habitat versus geographic cohesiveness: size and shape of Bembicium vittatum Philippi (Gastropoda: Littorinidae) in the Houtman Abrolhos Islands

In the Houtman Abrolhos Islands, Western Australia, the direct-developing littorine snail Bembicium vittatum occupies a wide range of habitats, which are replicated across the three major groups of islands. Earlier studies showed that allozyme similarities followed patterns related to gene flow, independent of habitat, providing an excellent opportunity to test for associations with habitat for traits more likely to be adaptively important. As the first test for adaptive divergence, we examined variation in size and shape of shells among 131 populations in the Abrolhos Islands. Two-fold variations were found in width of adults, the allometric coefficient of height with width, and shell height scaled to a standard width. Quantification of habitat characteristics was summarized by principal components analysis. In contrast with the patterns of divergence for allozymes, shell height, adjusted for width, was strongly associated with habitat: flatter shells are found on exposed, vertical shores, while domed, more globose shells predominate in sheltered sites. This association was stronger for shape of adult-sized snails than for height scaled to an arbitrary size, highlighting the importance of using biologically relevant measures. Even highly isolated and allozymically less variable populations in tidal ponds conformed to this association. Because differences in shape are highly heritable in B. vittatum , this association of shape with habitat, independent of patterns of gene flow, indicates local adaptation. Shell size also varied with habitat, but because growth rate is highly plastic, variation in size cannot be interpreted simply in terms of adaptation. Nevertheless, the pattern of variation indicates that, within realized limits, larger size is generally favourable, but may be constrained by local conditions. Thus, variation in size signals the potential for adaptive divergence of life histories among the many, isolated populations of this species.     

Response of hermit crabs to sinistral shells

Shell rotating behavior of the hermit crabPagurus geminus was investigated. In preliminary observations, hermit crabs motivated to change shells rotated presented shells, filled with sand, in a way that dislodged the inside material. In order to determine if this behavior is stereotyped, or flexible and dependent on shell type, hermit crabs were tested with ordinary dextral shells ofLatirulus nagasakiensis and sinistral shells ofAntiplanes contraria. Sinistral shells are not normally encountered by hermit crabs. Their rotation of the dextral shell to the left was adequate for sand discharge. Sinistral shells were rotated in both directions. Analysis of recorded videotapes showed that variation in rotation direction could be attributed to variation in the position of the crab relative to the shell. When the crab faced the shell aperture from the inner lip, it rotated the sinistral shell to the right, and to opposite direction when it faced from the outer lip side. The crab always pushed the upper side of the horizontally laid shell, regardless of shell type or its own position.     

New shell acquisition in the hermit crab,Pagurus geminus

The process of how the hermit crab,Pagurus geminus, acquires a new shell was investigated in the natural habitat at Ezura in Shirahama, Wakayama Prefecture, during the non-breeding season, and the following results were obtained. Hermit crabs acquired new shells most frequently by shell exchange between 2 individuals and occasionally by attacking snails. Acquisition through location of empty shells was not found. At the snail attacking site or the site of shell exchange attempts, sometimes many other individuals appeared and, frequently, confusing or complex shell changes were observed. The importance of introduction of fresh shells to a hermit crab population and the possibility for a certain individual to acquire a shell introduced by others through shell exchange attempts are discussed.