Temporal range: 136–0Ma
Hermit crabs are decapod crustaceans of the superfamily Paguroidea. Most of the 1100 species possess an asymmetrical abdomen which is concealed in an empty gastropod shell that is carried around by the hermit crab.
Most species have long, spirally curved abdomens, which are soft, unlike the hard, calcified abdomens seen in related crustaceans. The vulnerable abdomen is protected from predators by a salvaged empty seashell carried by the hermit crab, into which its whole body can retract. Most frequently hermit crabs use the shells of sea snails (although the shells of bivalves and scaphopods and even hollow pieces of wood and stone are used by some species). The tip of the hermit crab's abdomen is adapted to clasp strongly onto the columella of the snail shell.
As the hermit crab grows in size, it has to find a larger shell and abandon the previous one. This habit of living in a second hand shell gives rise to the popular name "hermit crab", by analogy to a hermit who lives alone. Several hermit crab species, both terrestrial and marine, use vacancy chains to find new shells: when a new, bigger shell becomes available, hermit crabs gather around it and form a kind of queue from largest to smallest. When the largest crab moves into the new shell, the second biggest crab moves into the newly vacated shell, thereby making its previous shell available to the third crab, and so on. Hermit crabs often "gang up" on a hermit crab that has what they perceive to be a better shell, where they will actually pry its home (shell) away from it and then compete for it, and one will ultimately take it over.
Most species are aquatic and live in varying depths of saltwater, from shallow reefs and shorelines to deep sea bottoms. Tropical areas host some terrestrial species, though even those have aquatic larvae and therefore need access to water for reproduction. Most hermit crabs are nocturnal.
Shells and shell competition
As hermit crabs grow they require larger shells. Since suitable intact gastropod shells are sometimes a limited resource, there is often vigorous competition among hermit crabs for shells. The availability of empty shells at any given place depends on the relative abundance of gastropods and hermit crabs, matched for size. An equally important issue is the population of organisms that prey upon gastropods and leave the shells intact. Hermit crabs that are kept together may fight or kill a competitor to gain access to the shell they favour. However, if the crabs vary significantly in size, the occurrence of fights over empty shells will decrease or remain non-existent.
A hermit crab with a shell that is too small cannot grow as fast as those with well-fitting shells, and is more likely to be eaten if it cannot retract completely into the shell. However, during times of molting, hermit crabs may temporarily move into a smaller shell, so that less sand comes through the opening when they bury themselves. The inverse has also been observed. Hermit crabs may move into a shell that is much too large to molt, especially if it is not able to bury itself in sand.
For some larger marine species, supporting one or more sea anemones on the shell can scare away predators. The sea anemone benefits, because it is in position to consume fragments of the hermit crab's meals. Other very close symbiotic relationships are known from encrusting bryozoans and hermit crabs forming bryoliths.
Development and reproduction
Hermit crab species range in size and shape, from species with a carapace only a few millimetres long to Coenobita brevimanus, which can live 30–70 years and can approach the size of a coconut. The shell-less hermit crab Birgus latro (coconut crab) is the world's largest terrestrial invertebrate.
The young develop in stages, with the first two (the nauplius and protozoea) occurring inside the egg. Most hermit crab larvae hatch at the third stage, the zoea. This is a larval stage wherein the crab has several long spines, a long narrow abdomen, and large fringed antennae. After several zoeal moults, this is followed by the final larval stage, the megalopa stage.
It is firmly established that hermit crabs are more closely related to squat lobsters and porcelain crabs than they are to true crabs (Brachyura). However, the relationship of king crabs to the rest of Paguroidea is a highly contentious topic. Many studies based on physical characteristics, genetic information and combined data support the longstanding hypothesis that the king crabs in the family Lithodidae are derived hermit crabs and should be classified as a family within Paguroidea. Other researchers have challenged this, asserting that Lithodidae (king crabs) should be placed with Hapalogastridae in a separate superfamily Lithodoidea. Six families are formally recognized in the superfamily Paguroidea, containing around 1100 species in total in 120 genera.
- Coenobitidae Dana, 1851 – 2 genera: terrestrial hermit crabs and the coconut crab
- Diogenidae Ortmann, 1892 – 20 genera of "left-handed hermit crabs"
- Paguridae Latreille, 1802 – 76 genera
- Parapaguridae Smith, 1882 – 10 genera
- Parapylochelidae Fraaije et al., 2012 – 2 genera
- Pylochelidae Bate, 1888 – 9 genera of "symmetrical hermit crabs"
- Pylojacquesidae McLaughlin & Lemaitre, 2001 – 2 genera
The fossil record of in situ hermit crabs using gastropod shells stretches back to the Late Cretaceous. Before that time, at least some hermit crabs used ammonites' shells instead, as shown by a specimen of Palaeopagurus vandenengeli from the Speeton Clay, Yorkshire, UK from the Lower Cretaceous.
Several marine species of hermit crabs are common in the marine aquarium trade. Of the approximately 15 terrestrial species in the world, the following are commonly kept as pets: Caribbean hermit crab (Coenobita clypeatus), Australian land hermit crab (Coenobita variabilis), and the Ecuadorian hermit crab (Coenobita compressus). Other species, such as Coenobita brevimanus, Coenobita rugosus, Coenobita perlatus or Coenobita cavipes, are less common but growing in availability and popularity as pets.
Hermit crabs are often seen as a "throwaway pet" that would live only a few months, but species such as Coenobita clypeatus have a 23-year lifespan if properly treated, and some have lived longer than 32 years.
In general, and despite their moniker, hermit crabs are social animals that do best in groups. In the wild they can be found in colonies of a hundred or more. Therefore, many sellers encourage the purchase of more than one crab. They also require a temperature- and humidity-controlled environment, and adequate substrate that is deep enough to allow them to completely bury themselves while moulting.
- Patsy McLaughlin & Michael Türkay (2011). "Paguroidea". In R. Lemaitre & P. McLaughlin. World Paguroidea & Lomisoidea database. World Register of Marine Species. Retrieved November 25, 2011.
- Patsy A. McLaughlin, Tomoyuki Komai, Rafael Lemaitre & Dwi Listyo Rahayu (2010). Part I – Lithodoidea, Lomisoidea and Paguroidea (PDF). In Martyn E. Y. Low and S. H. Tan. "Annotated checklist of anomuran decapod crustaceans of the world (exclusive of the Kiwaoidea and families Chirostylidae and Galatheidae of the Galatheoidea)". Zootaxa. Suppl. 23: 5–107.
- Ray W. Ingle (1997). "Hermit and stone crabs (Paguroidea)". Crayfishes, lobsters, and crabs of Europe: an illustrated guide to common and traded species. Cambridge University Press. pp. 83–98. ISBN 978-0-412-71060-5.
- Jason D. Williams; John J. McDermott (2004). "Hermit crab biocoenoses: a worldwide review of the biodiversity and natural history of hermit crab associates" (PDF). Journal of Experimental Marine Biology and Ecology 305: 1–128. doi:10.1016/j.jembe.2004.02.020.
- W. D. Chapple (2002). "Mechanoreceptors innervating soft cuticle in the abdomen of the hermit crab, Pagurus pollicarus". Journal of Comparative Physiology A 188 (10): 753–766. doi:10.1007/s00359-002-0362-2. PMID 12466951.
- Douglas Harper. "Hermit". Online Etymology Dictionary. Retrieved March 26, 2010.
- Borden, Kristin (1995). Vacancy Chains in the Hermit Crab, Pagurus Longicarpus. Tallahassee, Florida: Florida State University. p. 104.
- "Social networking helps hermit crabs find homes: previously unknown group behaviors lead to better housing for all". Tufts University. April 26, 2010.
- Randi D. Rotjan, Jeffrey R. Chabot & Sara M. Lewis (2010). "Social context of shell acquisition in Coenobita clypeatus hermit crabs". Behavioral Ecology 21 (3): 639–646. doi:10.1093/beheco/arq027.
- Robert Sanders (October 26, 2012). "Hermit crabs socialize to evict their neighbors". University of California, Berkeley.
- E. Tricarico & F. Gherardi (2006). "Shell acquisition by hermit crabs: which tactic is more efficient?". Behavioral Ecology and Sociobiology 60 (4): 492–500. doi:10.1007/s00265-006-0191-3.
- J. E. Angel (2000). "Effects of shell fit on the biology of the hermit crab Pagurus longicarpus (Say)". Journal of Experimental Marine Biology and Ecology 243 (2): 169–184. doi:10.1016/S0022-0981(99)00119-7.
- A. Klicpera, Paul D. Taylor, H. Westphal (2013). "Bryoliths constructed by bryozoans in symbiotic associations with hermit crabs in a tropical heterozoan carbonate system, Golfe d’Arguin, Mauritania". Marine Biodiversity. doi:10.1007/s12526-013-0173-4.
- P. Grubb (1971). "Ecology of terrestrial decapod crustaceans on Aldabra". Philosophical Transactions of the Royal Society B 260 (836): 411–416. Bibcode:1971RSPTB.260..411G. doi:10.1098/rstb.1971.0020.
- H. J. Squires (1996). "Larvae of the hermit crab, Pagurus arcuatus, from the plankton (Crustacea, Decapoda)". Journal of Northwest Atlantic Fishery Science 18: 43–56. doi:10.2960/J.v18.a3.
- J. D. MacDonald, R. B. Pike and D. I. Williamson (1957). "Larvae of the British Species of Diogenes, Pagurus, Anapagurus,and Lithodes". Proceedings of the Zoological Society of London 128: 209–257.
- C. W. Cunningham, N. W. Blackstone & L. W. Buss (1992). "Evolution of king crabs from hermit crab ancestors". Nature 355 (6360): 539–542. Bibcode:1992Natur.355..539C. doi:10.1038/355539a0. PMID 1741031.
- C. L. Morrison, A. W. Harvey, S. Lavery, K. Tieu, Y. Huang & C. W. Cunningham (2001). "Mitochondrial gene rearrangements confirm the parallel evolution of the crab-like form". Proceedings of the Royal Society B: Biological Sciences 269 (1489): 345–350. doi:10.1098/rspb.2001.1886. PMC 1690904. PMID 11886621.
- Ling Ming Tsang, Tin-Yam Chan, Shane T. Ahyong & Ka Hou Chu (2011). "Hermit to king, or hermit to all: multiple transitions to crab-like forms from hermit crab ancestors". Systematic Biology 60 (5): 616–629. doi:10.1093/sysbio/syr063. PMID 21835822.
- Patsy A. McLaughlin & Rafael Lemaitre (1997). "Carcinization in the anomura – fact or fiction? I. Evidence from adult morphology". Contributions to Zoology 67 (2): 79–123. PDF
- Sammy De Grave, N. Dean Pentcheff, Shane T. Ahyong et al. (2009). "A classification of living and fossil genera of decapod crustaceans". Raffles Bulletin of Zoology. Suppl. 21: 1–109.
- René H. B. Fraaije, Adiël A. Klompmaker & Pedro Artal (2012). "New species, genera and a family of hermit crabs (Crustacea, Anomura, Paguroidea) from a mid-Cretaceous reef of Navarra, northern Spain". Neues Jahrbuch für Geologie und Paläontologie 263 (1): 85–92. doi:10.1127/0077-7749/2012/0213.
- René H. Fraaije (2003). "The oldest in situ hermit crab from the Lower Cretaceous of Speeton, UK". Palaeontology 46 (1): 53–57. doi:10.1111/1475-4983.00286.
- Land Hermit Crab Care Guide. Pet Smart. 2006. Archived from the original on 2011-06-11.
- Linda Lombardi (July 22, 2008). "Hermit crabs don’t have to fade away; with proper care they can have long life". Amherst Daily News (The Associated Press). Retrieved July 2009.
- Stacy (February 21, 2013). "How old is my hermit crab?". The Crabstreet Journal. Retrieved April 28, 2013.
- Christa Wilkin (2004). "Basic crab care". Retrieved August 2008.
- Tammy Weick (2010). "The Hermit Crab Patch". Retrieved November 2010.