The effects of gastropod shell availability and habitat characteristics on shell utilization by the intertidal hermit crab Pagurus longicarpus Say

The shell utilization patterns of two intertidal populations of the hermit crab, Pagurus longicarpus Say, were studied. The populations differed with respect to the physical characteristics of their habitats and the availability of empty gastropod shells. The first population was in an estuary connected to Narragansett Bay. This population had few, if any. empty shells available in the area. The second population was in a rock-cobble area directly on Block Island Sound. There were large numbers of empty gastropod shells available for this population. The consistently high gastropod mortality on this shore appears to be caused by the animals being washed up on the beach, where they die due to desiccation.Data from samples collected from June to November of both 1974 and 1975 showed that there were distinct differences in the shell utilization patterns of the two populations. A greater proportion of the animals collected from the estuary population inhabited damaged shells and/or shells with symbionts compared to the individuals from the population with large numbers of empty shells available.The results of shell selection experiments indicated that individuals from both populations inhabited less than preferred shells. The population with large numbers of empty shells available was qualitatively shell-limited because of the effect of physical factors on the morphology of the gastropod species of that area. In addition, the shell selection experiments showed that individuals from the two areas had significantly different shell preferences. This result may be explained by the effects of the environment on the growth rates of the hermit crabs and/or as an indication that shell preferences may vary in response to the physical factors of a given habitat.     

Effects of trematode parasitism on the shell morphology of snails from flow and nonflow environments

The primary function of the gastropod shell is protection. However, shells that function well in one environment may be maladaptive in another. Upon infection, the snail shell protects internal parasites and it is to the parasite's advantage to optimize, or not interfere with, shell functionality. However, parasites, particularly trematodes, are often pathogenic and it is not clear if parasitism will induce environment‐dependent or ‐independent changes to gastropod shells. We conducted a field study and a complementary laboratory experiment to examine the effects of trematode parasitism on shell characteristics (shape, size, and crush resistance) of Physa acuta snails in flow and nonflow environments using geometric morphometrics and crush assays. Field results indicate wetland (nonflow) snails had large, crush resistant shells with narrow apertures and tall spires. In contrast, stream (flow) snails had small, weak shells with wide apertures and short spires. Parasitism had no apparent effect on the crush resistance of wetland snails but significantly reduced the crush resistance of stream snails. Parasitism had no significant effect on overall shell shape in stream or wetland snails. Similar to the results of our field study, nonflow tank snails had significantly more crush resistant shells than flow tank snails. Additionally, the shapes of flow and nonflow tank snails significantly differed where nonflow tank snails resembled wetland snails and flow tank snails resembled stream snails. For laboratory snails, parasitism reduced crush resistance regardless of flow/nonflow treatment. Our results demonstrate that habitat and/or flow treatment was the primary factor affecting P. acuta shell morphology and that trematode parasitism played a secondary role. J. Morphol. 277:316–325, 2016. © 2015 Wiley Periodicals, Inc.     

SHELL MICROSTRUCTURE OF GASTROPODS FROM LAKE TANGANYIKA,AFRICA: ADAPTATION,CONVERGENT EVOLUTION,AND ESCALATION

Gastropod shells from Lake Tanganyika, with their heavy calcification, coarse noded ribbing, spines, apertural lip thickening and repair scars, resemble marine shells more closely than they resemble other lacustrine shells. This convergence between Tanganyikan and marine gastropod shells, however, is not just superficial. Scanning electron microscope (SEM) studies reveal that the Tanganyikan shells are primarily layers of crossed-lamellar crystal architecture (that is, needle-like aragonite crystals arranged into laths that are packed into sheets such that the aragonite needles of adjacent laths are never parallel). The number of crossed-lamellar layers can vary from one to four between different Tanganyikan gastropod species. In species with two or more crossed-lamellar layers, the orientation of the lamellae is offset by approximately 90° between the different layers. The number of crossed-lamellar layers in the shell wall is positively correlated with shell strength and with predation resistance. Three and four crossed-lamellar layers in the shell wall evolved several times independently within the endemic thiarid gastropod radiation in Lake Tanganyika. Repeated origins of three and four crossed-lamellar layers suggest that they may be specific adaptations by Tanganyikan gastropods to strengthen their shells as a defense against shell-crushing predators.     

Ecological relations between hermit crabs and their shell-supplying gastropods: Constrained consumers

Hermit crabs are critically dependent upon gastropod shells for their survival and reproductive fitness. While anecdotal reports have suggested that hermit crabs may be capable of removing live gastropods from their shells to access the essential shell resource, no systematic experiments have been conducted to investigate this possibility. This paper reports experiments on both marine (Pagurus bernhardus) and terrestrial (Coenobita compressus) hermit crabs in which crabs were paired in the laboratory with the gastropods whose shells they inhabit in the field. Pairings included both shelled and naked crabs and spanned the full range of the gastropod life cycle. Neither marine nor terrestrial hermit crabs were successful at removing live gastropods from their shells. Furthermore, only a small fraction of the crabs (5.7%) were capable of accessing shells in which the gastropod had been killed in advance, with its body left intact inside the shell. Finally, although hermit crabs readily entered empty shells positioned on the surface, few crabs (14.3%) were able to access empty shells that were buried just centimeters beneath them. These results suggest that hermit crabs are constrained consumers, with the shells they seek only being accessible during a narrow time window, which begins following natural gastropod death and bodily decomposition and which typically ends when the gastropod's remnant shell has been buried by tidal forces. Further experiments are needed on more species of hermit crabs as well as fine-grained measurements of (i) the mechanical force required to pull a gastropod body from its shell and (ii) the maximum corresponding force that can be generated by different hermit crab species' chelipeds.     

What makes a good home for hermits? Assessing gastropod shell density and relative strength

The survival and reproductive success of hermit crabs is intrinsically linked to the quality of their domicile shells. Because damaged or eroded shells can result in greater predation, evaluating shell structure may aid our understanding of population dynamics. We assessed the structural attributes of Cerithium atratum shells through assessments of (a) density using a novel approach involving computed tomography and (b) tolerance to compressive force. Our goal was to investigate factors that may influence decision making in hermit crabs, specifically those that balance the degree of protection afforded by a shell (i.e. density and strength) with the energetic costs of carrying such resources. We compared the density and relative strength (i.e. using compression tests) of shells inhabited by live gastropods, hermit crabs (Pagurus criniticornis) and those found empty in the environment. Results failed to show any relationship between density and shell size, but there was a notable effect of shell density among treatment groups (gastropod/empty/hermit crab). There was also a predictable effect of shell size on maximum compressive force, which was consistent among occupants. Our results suggest that hermit crabs integrate multiple sources of information, selecting homes that while less dense (i.e. reducing the energy costs of carrying these resources), still offer sufficient resistance to compressive forces (e.g. such as those inflicted by shell-breaking predators). Lastly, we show that shell size generally reflects shell strength, thus explaining the motivation of hermit crabs to search for and indeed fight over the larger homes.     

Interference and exploitation components in interespecific competition between sympatric intertidal hermit crabs

This study was designed to evaluate the effect of interference and exploitation competition in shell partitioning between two hermit crab species (Pagurus criniticornis and Clibanarius antillensis). Field samples revealed that shells of the gastropod Cerithium atratum were the main resource used by both hermit crab species and that Pagurus used eroded or damaged shells in higher frequency than Clibanarius. The exploitative ability of each species was compared between species in the laboratory using dead gastropod (Cerithium) baits to simulate predation events and signalize newly available shells to hermit crabs. Pagurus reached the baits more rapidly than Clibanarius, but this higher exploitative ability did not explain shell utilization patterns in nature. Another experiment evaluated the dominance hierarchy between these two hermit crab species and revealed that Clibanarius was able to outcompete Pagurus for higher quality shells in agonistic encounters. This higher interference competitive ability of Clibanarius in relation to Pagurus may explain field observations. Nevertheless, Pagurus may be responsible to enhance shell availability to other hermit crab species that have lower ability to find and use newly available shells. Differently, the poorer condition of shells used by Pagurus, the higher ability of this species to attend gastropod predation events and its higher consumption rate by shell-breaking crabs (Menippe nodifrons) may increase its predation risks, thus revealing the disadvantages of such an exploitative competitive strategy for hermit crabs.     

Land hermit crab (Coenobita clypeatus) densities and patterns of gastropod shell use on small Bahamian islands

Aim To examine patterns of abundance, density, size and shell use in land hermit crabs, Coenobita clypeatus (Herbst), occurring on three groups of small islands, and to determine how these variables change among islands. Location Small islands in the Central Exuma Cays and near Great Exuma, Bahamas. Methods Land hermit crabs were captured in baited pitfall traps and were separately attracted to baits. A mark–recapture technique was used in conjunction with some pitfall traps monitored for three consecutive days. The size of each crab and the type of adopted gastropod shell were recorded, along with physical island variables such as total island area, vegetated area, island perimeter, elevation and distance to the nearest mainland island. Results Relative abundances, densities and sizes of crabs differed significantly among the three island groups. Densities of land hermit crabs were as high as 46 m⁻² of vegetated island area. In simple and multiple linear regressions, the only variable that was a significant predictor of the abundance of hermit crabs was the perimeter to area ratio of the island. Patterns of gastropod shell use varied significantly among the island groups, and the vast majority of adopted shells originated from gastropod species that inhabit the high intertidal and supratidal shorelines of the islands. Main conclusions Although densities of land hermit crabs varied, they were relatively high on many islands, and land hermit crabs may play an important role in these insular food webs. Patterns of shell use may be strongly restricted by island geomorphology: irregular shorelines provide relatively more habitat for the gastropod species that account for the majority of adopted shells and the steep sides of the islands prevent the accumulation of marine gastropod shells. The size of adult hermit crabs appears to be limited by the relatively small gastropod shells available, while the abundance of hermit crabs may be limited by the number of shells available.     

A Middle Devonian symbiotic relationship involving a gastropod, a trepostomatous bryozoan, and an inferred secondary occupant

Morris, P. J., Linsley, R. M. & Cottrell. J. F. 1991 01 15: A Middle Devonian symbiotic relationship involving a gastropod, a trepostomatous bryozoan. and an inferred sceondary occupant. Lethaia , Vol. 24. pp. 55–67. Oslo. ISSN 0024–1164.
The high-spired gastropod Palaeozygopleuru (Loxonematacea) of the Hamilton Group (Middle Devonian) in New York State is often entrusted by the trepostomatous bryozoan Leptotrypella (Hetero-trypidae). The form of this enerustation leads us to infer a secondary occupant that dwelled in empty shells of Palaeozygopleura while the bryozoan grew upon them. Encrusted specimens usually have an open aperture, thin or no enerustation on the apertural side of the gastropod shell. and thick encrustation on the abapertural side. While the aperture is invariably open. the columellar and parictal lips of the aperture, and the apertural face of the first whorl are usually encrusted. While the gastropod is alive, this area rests upon the dorsal surface of the foot and the remainder of the shell rests upon the substratc. These encrustation patterns suggest that an occupant of the shell. other than the gastropexl. prevented overgrowth of the aperture and oriented the shell aperture-down. This allowed ahapertural growth of the bryozoan. The presence of thin encrustation on the apertural side of the shell is problematical. It requires either the presence of a secondary occupant capable of holding a thinly encrusted shell off the substrate, or the ability of the juvenile bryozoan colony to extend onto portions of the shell that were in contact with the substrate. The presence of a secondary occupant. such as a sipunculan worm. capable of lifting the shell, but usually resting it aperture-down on the substrate seems the most suitable explanation for the nature of the encrustation. Gastropoda. bryozoa. symbiosis. Devoniun. hermit crab, Sipuncula     

Ocean Warming,More than Acidification,Reduces Shell Strength in a Commercial Shellfish Species during Food Limitation

Ocean surface pH levels are predicted to fall by 0.3–0.4 pH units by the end of the century and are likely to coincide with an increase in sea surface temperature of 2–4°C. The combined effect of ocean acidification and warming on the functional properties of bivalve shells is largely unknown and of growing concern as the shell provides protection from mechanical and environmental challenges. We examined the effects of near-future pH (ambient pH –0.4 pH units) and warming (ambient temperature +4°C) on the shells of the commercially important bivalve, Mytilus edulis when fed for a limited period (4–6 h day⁻¹). After six months exposure, warming, but not acidification, significantly reduced shell strength determined as reductions in the maximum load endured by the shells. However, acidification resulted in a reduction in shell flex before failure. Reductions in shell strength with warming could not be explained by alterations in morphology, or shell composition but were accompanied by reductions in shell surface area, and by a fall in whole-body condition index. It appears that warming has an indirect effect on shell strength by re-allocating energy from shell formation to support temperature-related increases in maintenance costs, especially as food supply was limited and the mussels were probably relying on internal energy reserves. The maintenance of shell strength despite seawater acidification suggests that biomineralisation processes are unaffected by the associated changes in CaCO₃ saturation levels. We conclude that under near-future climate change conditions, ocean warming will pose a greater risk to shell integrity in M. edulis than ocean acidification when food availability is limited.     

Do predatory drill holes influence the transport and deposition of gastropod shells?

Predatory gastropod drill holes are an abundant and easily identifiable signal of predation in ancient and modern molluscan shell assemblages. Many workers have used drill holes to interpret patterns of predation intensity and success in fossil assemblages. These studies are predicated on the assumption that the relative abundances of drilled and undrilled shells in an assemblage accurately reflect those of the community from which the shells were originally derived. The underlying assumption is that drilled and undrilled shells are transported into shell accumulations in the same manner. If this assumption is false, shell accumulations do not represent taphonomically unbiased samples, but rather preferentially sorted deposits from which conclusions about drilling predation cannot be made. To test the hypothesis that drilled and undrilled gastropod shells transport at different flow velocities, multiple transport trials were conducted on two morphologically distinct taxa, Olivella biplicata and Euspira lewisii. Individual specimens were placed in a recirculating flume tank and observed from rest (in stable orientation) until they were transported downstream. During each trial, flow velocity was slowly and incrementally increased, so as to avoid pulses of acceleration, until shells began to move downstream. Drilled and undrilled specimens of both taxa demonstrate statistically significant correlations between shell mass and average transport velocity. Similarly sized drilled and undrilled specimens of both taxa do not exhibit significant differences in transport velocity. These results indicate that predatory drill holes do not change the hydrodynamic properties of gastropod shells. Therefore, gastropod shell assemblages are not likely to be affected by differential transport and sorting of drilled and undrilled shells.     

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.     

Continuous growth-line sequences in gastropod shells

Studies of gastropod shell growth at the level of fine growth layers are scarce, because coiling of gastropod shells hinders the observation of continuous growth series spanning across whorls. We propose here a new method to obtain continuous growth patterns of gastropod shells over whorls with Terebralia palustris (L.) as an example. Comparison of vertical and horizontal sections of the shell of this species reveals that growth patterns can be observed continuously for several whorls on the vertical section of the columella. In addition, an obvious tidal growth pattern preserved in this species enables us to trace its growth with a precision of 12.4 h and indicates that it takes about two years for a shell to grow from 3 cm to 9.5 cm in height and add 5 complete whorls.     

Larval and juvenile gastropods from a Carboniferous black shale: palaeoecology and implications for the evolution of the Gastropoda

A horizon in the late Visean Ruddle Shale from Arkansas contains the oldest well-preserved gastropod protoconchs known from the Americas. The gastropod fauna consists of a diverse larval shell assemblage and a low diversity assemblage of juvenile gastropods that probably had a benthic life habit. Gastropod larval shells are always isolated, i.e. the gastropods did not complete their life cycle (no metamorphosis) and were unable to become benthic. This was caused by unfavorable environmental conditions on the soft muddy bottom that was probably due to anaerobic to exaerobic conditions. The absence or scarcity of bioturbation caused by invertebrate detritus or sediment feeders in both shale and concretions (formed before compaction) favored preservation of the delicate larval shells. The lack or scarcity of infauna and bioturbation as well as the low diversity of the presumed benthos supports an interpretation of a quasi-anaerobic to exaerobic benthic environment. The superbly preserved larval shells demonstrate that there are more caenogastropod clades present in the late Palaeozoic than suggested previously. Some larval shell types have an openly coiled first whorl followed by a planktotrophic larval shell; openly coiled initial whorls are unknown from modern caenogastropods. The vetigastropods have a smooth protoconch of two whorls clearly demarked from the following whorls - a pattern unknown in modern vetigastropods which have a protoconch of less than one whorl and build no larval shell during their planktonic stage. This could indicate a link between Palaeozoic vetigastropods and the caenogastropods.     

Reproduction and larval development of Polydora robi (Polychaeta: Spionidae), an obligate commensal of hermit crabs from the Philippines

Abstract. The reproduction of a recently described spionid polychaete, Polydora robi , is examined from the Philippines. Adults inhabit a burrow in the apex of gastropod shells occupied by hermit crabs. Females were found to deposit broods of 18–94 egg capsules in the summer (June–August) and winter months (January–March) sampled. Paired or single egg capsules are attached by stalks to the inside wall of the burrow and contain 40–106 eggs which average 97 μm in diameter. The total number of eggs per brood ranges from 941–8761 eggs and is positively correlated with the total number of segments and length of female worms. Adults of P. robi are polytelic, producing ≤9 successive broods over a 3-month period; a mean of 6.7 d was exhibited between broods in the laboratory. Females utilize sperm stored in the seminal receptacles during successive spawnings. Development occurs within egg capsules until the 3-segment stage, at which time the planktotrophic larvae are released. Juveniles of ∼20 segments are competent to settle on gastropod shells inhabited by hermit crabs. Members of P. robi are relatively fecund, semicontinuous breeders; the life-cycle in this species is similar to the only other known obligate polydorid commensal of hermit crabs.     

Some Aspects of Hole-Boring Predation by Octopus vulgaris

Octopus vulgaris prey upon many gastropod species by boringholes in the shell, weakening the prey with a venom, removingthe entire prey, and eating it. When offered Strombus raninusthe Octopus quickly grasped the conch with one or a few arms,checked for occupancy by inserting an arm tip into the aperture,and passed the shell under the web to the mouth. The shell washeld against the buccal mass by the circumoral suckers and raspedrepeatedly with the radula, repositioned, and rasped again.There were brief pauses of apparent inactivity between the periodsof active rasping. The shell was penetrated at an approximatemaximal rate of 1.25 mm per hour. The boreholes averaged 0.93mm in outer diameter, 0.47 mm in inner diameter and 0.88 mmin depth. The boreholes were extremely variable in shape, size,and position on the spire. There was a marked preference forindividual animals to bore in a particular sector of the spire.Apparently the animals orient the shells by using the lip asa point of reference because lipless shells had the boreholesrandomly distributed around the shell.     

Symbiosis between gastropods and bryozoans in the late Ordovician of Cumbria, England

Five examples of symbiosis between gastropods and trepostome bryozoans are described from the Ashgill (late Ordovician) of Cumbria (England). The gastropods are invariably found associated with the bryozoans. whereas the bryozoans may be free-living. Encrustation is considered to have taken place, in most cases, on mature, living gastropod shells, resulting in the trepostome utilizing the shell as a surrogate basal disc. Three specimens show encrustation on an empty gastropod shell, causing the trepostome to develop a basal disc similar to non-encrusting forms. The bryozoan colony probably benefited from the symbiotic relationship by increased water flow over the colony, caused by gastropod locomotion, whereas the gastropod was afforded protection from predators. The new species Spiroecus nidhoeggi. Diplotrypa hvergelmi and Monotrypa fontinalis are described.     

Avoidance of drilled gastropod shells by the hermit crab Pagurus longicarpus at Nahant, Massachusetts

Most hermit crabs depend on empty gastropod shells for shelter; competition for appropriate shells is often severe. This study determined whether shells that have been drilled by naticid gastropods are suitable for occupancy by the hermit crab Pagurus longicarpus. Differences in the characteristics of empty shells and those occupied by hermit crabs were assessed at two adjacent field sites in Nahant, Massachusetts. Drilling damage was far more frequent in empty gastropod shells than in shells occupied by hermit crabs, suggesting that individuals of P. longicarpus avoid drilled shells. They did not appear to avoid shells with other forms of damage. Laboratory experiments confirmed that these hermit crabs preferentially chose intact shells over drilled shells, even when the intact shells offered were most suitable for crabs half the weight of those tested. Final shell choices were generally made within 1 h. The hermit crabs apparently discriminated between intact and drilled shells based on tactile cues, since crabs kept in the dark showed the same preference for intact shells. The hermit crabs strongly avoided, to nearly the same extent, artificially drilled shells, naturally drilled shells, and shells with holes artificially drilled on the opposite side of the shell from where they would normally be located. Possible selective forces causing P. longicarpus to show such strong behavioral avoidance of drilled shells include increased vulnerability of crabs in drilled shells to osmotic stress, predation, and eviction by conspecifics.     

Crab shell-crushing predation and gastropod architectural defense

The shell-breaking behavior of the crabs Ozius verreauxii Saussure 1853 and Eriphia squamata, Stimpson 1859 from the Bay of Panama is described. The master claws of both these crabs are well designed for breaking shells. Small shells, relative to the size of a crab predator, are crushed by progressively breaking off larger segments of a shell's apex, while larger shells are peeled by inserting a large dactyl molar into the aperture of a shell and progressively chipping away the lip of the shell.

Heavy gastropod shells are shown to be less vulnerable to crab predators than lighter shells, and narrow shell apertures and axial shell sculpture are demonstrated to be architectural features that deter crab predation. The incidence of architectural features which deter crab predation appears to be higher for smaller gastropod species than for larger gastropods which are too large for most crab predators. Large fish predators prey upon both gastropods and shell-crushing crabs. To avoid fish predators, both these prey groups seek refuge under rocks when covered by the tide. Fish predation thus appears to enforce a close sympatry between smaller gastropods and their crab predators.     

How do gastropods grow synchronized shell sculpture? Effect of experimental varix manipulations on shell growth by Ceratostoma foliatum (Muricidae: Ocenebrinae)

Gastropod shells display striking patterns in both color and sculpture, but rather little is known about the developmental mechanisms that produce those patterns. Here, we tested a physical feedback hypothesis for how snails control spatial patterning of shell sculpture. Varices—a form of synchronized, blade‐like axial sculpture—are produced at regular intervals around the shell and often aligned closely between adjacent whorls. Older varices were believed to provide a spatial cue about where to position a new varix. To test this hypothesis, we manipulated physical cues by cutting off varices or attaching new ones to the body whorl of individuals of Ceratostoma foliatum, and then allowing snails to grow a new varix. We found that previous varices on the shell were neither necessary nor sufficient to induce a new varix at a particular location. However, the position of older varices did appear to affect the fine tuning of subsequent varix placement. The results of our experiments therefore suggest that varix synchrony arises mainly from some internal mechanism that yields a standardized amount of spiral growth per growth spurt. We also found that shell damage can induce varix production in unusual or aberrant locations during subsequent shell growth.     

Gastropod shells: A potentially limiting resource for hermit crabs

The availability of gastropod shells to hermit crabs in the Newport River Estuary, Beaufort, N.C. has been assessed by determining the numbers of usuable shells occurring in characteristic subtidal habitats and by measuring shell size adequacy. The proportion of useable shells occupied by hermit crabs ranged from 58–99 % and many of the shells not used by hermit crabs were judged unavailable because they were occupied by sipunculids or only uncovered by the dredge. The shell adequacy index (shell size occupied/shell size preferred) was significantly below 1.0 for the largest species (Pagurus pollicaris Say) in the one location where sufficient numbers were collected and for the next largest species (P. longicarpus Say) in three of the four locations where it was collected. The shell size adequacy index for the smallest species (P. annulipes Stimpson) did not differ significantly from 1.0 in either of the two locations in which it was found. These observations suggest that the availability of gastropod shells plays a significant rôle in limiting the abundance of at least the larger hermit crabs.