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.     

Hermit crab biocoenoses: a worldwide review of the diversity and natural history of hermit crab associates

The symbiotic associates of hermit crabs (excluding parasites and flora) are reviewed worldwide. The review includes species found on the shells occupied by hermit crabs (epibiotic species), species boring into these shells (endolithic species), species living within the lumen of the shell (either free-living or attached to the shell), species attached to the hermit crabs themselves, and hypersymbionts. In total over 550 invertebrates, from 16 phyla are found associated with over 180 species of hermit crabs. Among these associates, 114 appear to be obligate commensals of hermit crabs, 215 are facultative commensals, and 232 are incidental associates. The taxa exhibiting the highest number of associates are arthropods (126), polychaetes (105), and cnidarians (100). The communities of species associated with Dardanus arrosor, Paguristes eremita, Pagurus bernhardus, Pagurus cuanensis, and Pagurus longicarpus are the best studied and harbor the most diverse assemblages of species. While trends in biodiversity of hermit crab assemblages do not follow predicted patterns (e.g., hermit crabs within the Indo-West Pacific do not harbor more species than those from temperate regions), this is suggested to reflect a lack of sampling rather than a true representation of the number of associates. Hermit crabs date to at least the Cretaceous and provided a niche for a number of groups (e.g., hydractinians, bryozoans, polydorids), which were already associates of living gastropods. Apparently hermit crab shells initially supplied a substrate for settlement and then these symbiotic relationships were reinforced by enhanced feeding of symbionts through the activity of the hosts. Through their use and recycling of gastropods shells, hermit crabs are important allogenic ecosystem engineers in marine habitats from the intertidal to the deep sea. Hermit crabs benefit from some symbionts, particularly cnidarians and bryozoans, through extension of shell apertures (alleviating need to switch into new shells) and by providing protection from predators. However, hermit crabs are also negatively impacted (e.g., decreased reproductive success, increased predation) by some symbionts and a review of egg predators is provided. Thus, the symbiotic relationships between hermit crabs and many associates are difficult to characterize and often exhibit temporal changes depending on environmental and biological factors. Research on the biology of these symbionts and the costs/benefits of their associations with hermit crabs are analyzed. While some associates (e.g., Hydractinia spp.) have been studied in considerable detail, for most associations little is known in terms of the impacts of symbionts on hosts, and future experimental studies on the multitude of relationships are suggested.     

Effect of gastropod shell characteristics and hermit crabs on shell Epifauna

The epifauna on gastropod shells occupied by the hermit crabs Pagurus pollicaris (Say) and P. longicarpus (Say) was examined, as was the utilization of shells by these two hermit crabs. In the study area in Tampa Bay, Florida, shells were not a limiting factor to the hermit crab population, and there apparently was little competition for shells. Interspecific competition for shells was limited because the two hermit crab species differed in size and hence occupied shells of different sizes. The total number and density of most epifaunal species were higher on shells occupied by hermit crabs than on unoccupied shells, possibly because hermit crabs prevent their shells from being buried and hence lengthen the time the epifaunal community can grow and develop. The hermit crab species also appeared to affect the epifaunal community, for the total number and density of most epifaunal species were larger on shells occupied by P. pollicaris than P. longicarpus. With increasing shell size, the populations of most epifaunal species, also were larger but not their density. Least influential in affecting the epifaunal community was the species of shells.     

Symbiosis of sea anemones and hermit crabs: different resource utilization patterns in the Aegean Sea

The small-scale distribution and resource utilization patterns of hermit crabs living in symbiosis with sea anemones were investigated in the Aegean Sea. Four hermit crab species, occupying shells of nine gastropod species, were found in symbiosis with the sea anemone Calliactis parasitica. Shell resource utilization patterns varied among hermit crabs, with Dardanus species utilizing a wide variety of shells. The size structure of hermit crab populations also affected shell resource utilization, with small-sized individuals inhabiting a larger variety of shells. Sea anemone utilization patterns varied both among hermit crab species and among residence shells, with larger crabs and shells hosting an increased abundance and biomass of C. parasitica. The examined biometric relationships suggested that small-sized crabs carry, proportionally to their weight, heavier shells and increased anemone biomass than larger ones. Exceptions to the above patterns are related either to local resource availability or to other environmental factors.     

A forced association between the slippersnail Crepidula convexa and the hermit crab Pagurus longicarpus?—possible influence from a third party

The suspension-feeding slippersnail Crepidula convexa is commonly associated with hermit crabs (Pagurus longicarpus) living in periwinkle shells (Littorina littorea) at our study site in Nahant, MA, USA. In 15 field surveys conducted at Nahant in 2000, 2001 and 2003, we found that (1) more than 61.8% of individuals of C. convexa resided on shells occupied by hermit crabs, as opposed to the shells of live periwinkles, empty periwinkle shells or other solid substrates; (2) an average of 8.3% of hermit crabs carried at least one individual of C. convexa; and (3) 39.1-75.0% of hermit crabs carrying C. convexa were carrying “large” individuals (snails with wet weight >10% of the weight of the periwinkle shells they occupied). However, it is unlikely that individuals of C. convexa seek out shells occupied by hermit crabs to colonize, and they showed no preference for empty periwinkle shells over other solid substrates in the laboratory. Moreover, in the laboratory the hermit crabs preferentially occupied intact shells bearing individuals of C. convexa only when the alternatives were shells that had been drilled by naticid snails. Thus, neither party preferentially associates with the other: rather, extensive predation by naticid snails on periwinkles at Nahant appears to limit the availability of suitable shells for the hermit crabs, forcing them to inhabit shells bearing “large” individuals of C. convexa. Individuals of C. convexa may benefit from this inadvertent association with hermit crabs: by facilitating snail dispersal, transport by hermit crabs should reduce the potential for inbreeding, an important consideration for a species that lacks free-living larvae in its life history.     

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.     

Evolutionary palaeoecology of symbioses between bryozoans and hermit crabs

Modern hermit crabs form associations with many organisms which encrust, bore into, or cohabit the living chambers of gastropod shells occupied by the crabs. Among these hermit crab symbionts are bryozoan species which develop massive, commonly multilayered, colonies encrusting hermit crab shells. These colonies extend the living chamber of the crab through a characteristic process of helicospiral tubular growth originating from the shell aperture. The scant information available on the ecology of Recent bryozoan‐hermit crab symbioses is reviewed. Symbioses have been recorded from intertidal to upper slope environments, and from tropical to cold temperate zones. None of the hermit crab species are obligatory symbionts of bryozoans, and the majority of the modern bryozoan species involved are also not obligatory symbionts. Fossil examples always lack the hermit crabs, which have a poor fossilization potential; however, the distinctive tubular growth pattern and other features of the bryozoans enable recognition of ancient examples of the symbiosis. The earliest inferred associations between bryozoans and hermit crabs date from the Mid Jurassic, but associations remained uncommon until the Neogene. A remarkably wide taxonomic diversity of Recent and fossil bryozoans are known or inferred symbionts of hermit crabs. The broad evolutionary pattern of the association demonstrates multiple originations of the symbiosis by bryozoans belonging to at least 5 cyclostome and 12 cheilostome families. Only the Miocene‐Recent cheilostome family Hippoporidridae has an evolutionary history closely tied to symbiosis with hermit crabs. There is no evidence for coevolution.     

Systematics and Ecology of Shell-Boring Polychaetes from New England

In a survey of shell-boring polychaeles of New England, representativesof five families were found: Spionidae, Cirratulidae, Capitellidae,Terebellidae, and Sabellidae. The five spionid species were studied extensively. These includePolydora commensalis Andrews, found only in shells occupiedby hermit crabs, P. concharum Verrill, P. socialis (Schmarda), P. websleri Hartman, and Boccardia hamata (Webster) , foundin various types of shell. Breeding periods were defined andthe larval development described for each species. Polydoraconcharum deposits egg capsules inwinter months, while the oilierpolydorids spawn in spring or summer. Morphology of planktoniclarvae is distinct in each species, although P. websteri larvaemay be confused with non-boring species such as P. ligni Webster.Polydora socialis adults are found in both shells and sedimentand have a unique grinding apparatus, a gizzard, between theesophagus and intestine. The cirratulid, Dodecaceria sp., follows an asexual mode ofreproduction. The syslematics of Dodecaceria is complex owingto multiple modes of reproduction. No sexually mature individualswere observed during the course of this study. Asexual budswerefound in the Fall. A sabellid, Pseudopolamilla reniformis (Miiller), is commonlyfound in theshells of Placopeclen magellanicits (Gmelin) inMaine waters. Its reproductionis unknown.     

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.     

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.     

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.     

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.     

Substratum and morphometric relationships in the bryozoan genus Odontoporella, with a description of a new paguridean-symbiont species from New Zealand

Members of the bryozoan family Hippoporidridae have frequently been found encrusting gastropod shells inhabited by hermit crabs, with which they appear to enter into a symbiotic relationship-shells occupied by hermits may in some species have a tubular extension of the encrusting bryozoan from the shell opening, induced by the presence of the crab. Such colony growth is characteristic of some species of Hippoporidra Canu and Bassler and Odontoporella Héjjas. The type species of Odontoporella, O. adpressa (Busk), has been attributed a nominal distribution from Chiloe Island, Chile (the type locality), to the Falkland Islands, New Zealand, and New Caledonia. In New Zealand, colonies are relatively easily obtainable from some localities, so a study was undertaken to ascertain substratum and morphometric relationships across the range of distribution of the species, using museum specimens and, where possible, fresh material. It became clear that the New Zealand population constitutes a separate species, here named O. bishopi n. sp., in which the orifice is proportionately larger than in O. adpressa. In contrast to O. adpressa, which settles on a range of substrata, O. bishopi preferentially settles on gastropod shells occupied by hermit crabs (mostly Paguristes setosus (H. Milne Edwards)) and shows sexual dimorphism at the level of the polypide. Male polypides not only have modified lophophores but also reduced guts.     

Larval release behaviors of the striped hermit crab, Clibanarius vittatus (Bosc): Temporal pattern in hatching

Ovigerous hermit crabs, Clibanarius vittatus (Bosc), were examined in the laboratory to (1) determine if the time of larval release is a synchronous event, (2) determine the influence of a damaged gastropod shell during the egg hatching process, and (3) describe larval release behaviors. Ovigerous hermit crabs from natural light:dark (LD) and tidal cycles were moved to constant conditions 2-3 days prior to the predicted time of larval release. Larval release was synchronous, occurring near the time of expected sunset. Females with early-stage embryos placed under constant conditions displayed a free-running circadian rhythm, suggesting that the rhythm is under endogenous control. Hermit crabs with early-stage embryos that were placed under a shifted LD cycle (advanced 12 h relative to the ambient photoperiod) before being placed under constant conditions advanced their larval release rhythm by 12 h, indicating the rhythm can be entrained by the LD cycle. Hermit crabs with an intact shell released larvae in bursts at sunset over several consecutive nights (period = 24.2 h). In contrast, hermit crabs with damaged shells released larvae at different times over the course of a single day. Ovigerous females with intact shells exhibit several stereotypical hatching behaviors. The female stands on her walking legs and thrusts her abdomen, moving the shell in an oscillating motion. This movement may assist in breaking the outer membrane of the egg case. The female generates a water current inside the shell with her scaphognathite and mouthparts, which transports the newly hatched larvae out of the shell. Females in damaged shells did not display these behaviors; instead, larval release was a prolonged event with little movement of the female, and often the newly hatched larvae were not viable. These results indicate that an intact shell plays an important role in the hatching process for this hermit crab.     

Examining the impact of a symbiotic lifestyle on the fecundity of the marine gastropod Crepidula plana

The marine gastropod Crepidula plana has an extensive latitudinal range along the eastern coast of the United States. It is usually found living within gastropod shells occupied by hermit crabs, although individuals can sometimes also be found living on rocks and on the exposed surfaces of shells. Our study sought to determine the extent to which residing inside periwinkle (Littorina littorea) shells occupied by the hermit crab Pagurus longicarpus at a study site in coastal Massachusetts compromises the fecundity of C. plana, through size limitation. The egg masses of symbiotic and free‐living females of C. plana included comparable numbers of egg capsules and embryos per female despite the smaller sizes of the symbionts; symbiotic females compensated for their smaller size by producing significantly more embryos per milligram of female body tissue than their free‐living counterparts. These data raise interesting questions about why—unlike its congener C. fornicata—C. plana has not yet become a successful invasive species.     

Biological features of a puzzling symbiotic association between the hermit crab Dardanus insignis and the porcellanid crab Porcellana Sayana (Crustacea)

The symbiotic lifestyle is widespread among porcellanid crabs, which maintain ecological and co-evolutionary associations with annelid polychaetes, poriferans, cnidarians, echinoderms, gastropod mollusks, and other crustaceans such as shrimps and hermit crabs, among others. We investigated the ecological association between the hermit crab Dardanus insignis and the porcellanid Porcellana sayana, in southeastern Brazil. Porcellanid crabs, hermit crabs, and available shells were collected monthly from July 2001 to June 2003, with a shrimp boat equipped with two double-rig trawl nets. The majority of P. sayana specimens were collected in shells occupied by D. insignis (96.6%); a few were found in empty shells (3.4%). The catch of both symbionts and hosts increased with increasing depth, with the highest occurrence at 35 m. The P. sayana crabs of various sizes could be found solitary or forming aggregations of up to 14 individuals per host, showing no sex or size segregation. In spite of the high diversity of shell species occupied by the hermit crabs and also available in the field, only a few of them were also utilized by P. sayana. The majority (93%) of shells utilized by P. sayana also hosted other symbiont species, constituting the basis of extensive symbiotic complexes. Thus, the ecological relationship between D. insignis and P. sayana may be classified as a non-obligate and non-specific symbiosis that may also involve other facultative organisms such as sea anemones.     

Quality of shells occupied by the hermit crabPagurus geminus: How many hermit crabs are satisfied with their shells?

The rate of changing shells in the hermit crabPagurus geminus was investigated to determine how many hermit crabs are satisfied with their shells. Animal collected from the coast of Oya, Tanabe, Wakayama Prefecture, were presented with fresh gastropod shells newly made by removing the soft parts. Approximately 80% of the hermit crabs changed from their original shells acquired in the natural habitat into fresh shells experimentally given to them and, thus, were regarded as dissatisfied with the shells possessed in the natural habitat. This condition was thought to lead to the fact that hermit crabs occasionally attempted to exchange shells between 2 individuals and even to attack living snails in the natural habitat.     

Shell preference and utilization patterns in littoral hermit crabs of the bay of Panama

Shell utilization patterns of three sympatric hermit crab species from the Bay of Panama are examined. Shell preferences, as shown by laboratory choice experiments and the selective use of empty shells experimentally added to hermit crab populations, are shown to be important determinants of shell utilization under natural conditions.Factors which influence the types and sizes of shells occupied by hermit crabs in separate populations include: (1) the presence and relative abundance of different gastropod species; (2) the specific shell preferences of different hermit crab species; and (3) the presence and relative abundance of sympatric hermit crab competitors for the limited supply of empty shells. Since the size and type of shell occupied by a hermit crab influences its growth rate and reproductive output, these factors appear to have a direct effect on hermit crab fitness and the demographic structure of separate hermit crab populations.     

Antipredator defence of the hermit crab Pagurus filholi induced by predatory crabs

Hermit crabs have two antipredator tactics: taking refuge in its shell and fleeing. We examined the following two hypotheses using the hermit crab Pagurus filholi : (1) hermit crabs change their preference for shell types that they take refuge in and/or change the timing of fleeing (i.e. the duration of refuge in the shell) when they perceive a predator threat; (2) the type of shell that a hermit crab occupies affects the fleeing tactic of the individual. Under the stimulus of a crushed conspecific, hermit crabs changed neither their preference for shell species nor their refuge duration. On the other hand, under the stimulus of the predatory crab Gaetice depressus , hermit crabs increased their preference for Batillaria cumingi shells, which provide superior protection against predators, and shortened their refuge duration in the shells even when they occupied those effective against predation. Refuge duration was longer in B. cumingi shells than in the more vulnerable shells of Homalopoma sangarense . These results suggest that both antipredator defences (changing shell and timing of fleeing) are induced by the stimulus of a predator, and the timing of fleeing is affected by the shell type occupied.     

Predation on symbiont sea anemones by their host hermit crab Dardanus pedunculatus

Feeding by host hermit crabs Dardanus pedunculatus on their symbiotic sea anemones Calliactis polypus was investigated using animals collected at Shirahama, Wakayama Prefecture, Japan. In the first experiment, changes in the number of sea anemones on hermit crab shells were recorded in single‐and double‐crab trials without food and single‐crab trials with food. The number of sea anemones significantly decreased under starved conditions. The extent of this decrease per single hermit crab was higher in the double‐crab trials than in the single‐crab trials. Direct observations and video recordings showed that hermit crabs occasionally removed sea anemones from their own shells, and also from partners’ shells in the double‐crab trials, and consumed them. In the second experiment, fed and unfed hermit crabs with or without sea anemones were examined for body weight changes. Fed hermit crabs gained weight whereas unfed hermit crabs lost it. The degree of weight loss in unfed hermit crabs was significantly higher in those without sea anemones, which indicates some value of the latter as food. We offer some speculations on the course of development of this symbiosis, with predation on sea anemones having played an important initial role.