Pagurus acadianus

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Pagurus acadianus
Pagurus acadianus.png
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Malacostraca
Order: Decapoda
Suborder: Pleocyemata
Infraorder: Anomura
Family: Paguridae
Genus: Pagurus
Species:
P. acadianus
Binomial name
Pagurus acadianus
J. E. Benedict, 1901

Pagurus acadianus, the Acadian hermit crab, is a species of hermit crab in the family Paguridae. [1] [2] [3] [4] It is found in Western Atlantic Ocean. [1]

Contents

Distribution

The Acadian hermit crab, also known as Pagurus acadianus, can be found in the Western Atlantic Ocean, including areas such as the Vineyard Sound. [5] In addition, the Acadian hermit crab has been cited as the most abundant species of crab in Salisbury Cove, Maine by William C. Grant, Jr, during his extensive study of hermit crabs populating this area in 1961. [6]

History

Pagurus acadianus was first identified in scientific literature by scientist J.E. Benedict in 1901. As examined by Morris H. Roberts, Jr.’s, Benedict was able to differentiate this organism from that of a very similar taxa, Pagurus benhardus, due to physical variations. Benedict observed that Pagurus acadianus had larger eyestalks, shorter fingers of the chelae and sharper chelipeds, all of which are necessary identifiers of the Acadian hermit crab. [7] Taxonomically, the Acadian hermit crab belongs to the Arthropoda phyla. Arthropods belong to the most populous animal phylum, with a recorded million (and counting) species. Arthropods include crustaceans and insects, and are characterized by the breadth of their variation in morphology, or their relationship among similar organisms based on comparisons between physical, chemical and taxonomic similarities. This can often be seen through the use of phylogenetic trees and cladograms. The Acadian hermit crab belongs to the Pagurus genera, along with the hairy hermit crab, or Pagurus pubescens, and the aforementioned Pagurus bernhardus . The abundance of their populations is seasonally dependent, with a peak in richness in the month of June, and a staggering decrease from the months of November to March. [5]  In addition, they are most plentiful in seawater temperatures ranging from 32 degrees Fahrenheit to 41 degrees Fahrenheit. [8] The Acadian hermit crab has most often been observed in its fossilized state, with 95.4% of occurrences being recorded as preserved specimen. With only 4.4% of occurrences being living organisms, there is much to know about this creature, and whether its ecological niche is similar to that of its common ancestors. [9]

Reproduction and development

Though very little is known on the specific reproductive behavior of Pagurus acadianus, information on their adolescence was attained by Roberts during his laboratory studies of this species. Roberts found that the incubation period of the larva is approximately 30 days, and the optimal temperature during gestation is 55.4 degrees Fahrenheit. Once they hatch, the size of the eggs is about 0.58 by 0.64 millimeters, and can be distinguished by varying hues of red and yellow coloration, in addition to distinctive eyespots. Both larval and adult Acadian hermit crabs are often confused with the closely related Pagurus berhnardus , or the common marine hermit crab of western Europe, and this comparison has been the focal point of many scientific evaluations, as demonstrated by Benedict's work. [7]

Habitat

As examined by Jennifer E. Angel in her paper, hermit crabs are known to inhabit different shells throughout their lifetimes, switching from shell to shell as a result of growth. Increased growth means increased shell size, because inhabiting a shell that is too small for the crab's body results in an increase in predation and desiccation. [10] Pagurus acadianus are often found inhabiting the shells of Littorina littorea, Thais lapillus, Buccium undatum, and Polinices heros , as concluded by William C Grant, Jr. Larger individuals are often located on elevated areas within the rocky intertidal, which is defined as the area between the highest high tides and the lowest low tides. [6] This area is one of much scientific exploration, due to its accessibility and the adaptations of the organisms that live there. These organisms have to face daily variation in salinity, exposure to sunlight and lack of food. Small individuals can be found on wharf piling and vertical faces of rock. This area can also be defined as the midway region of the rocky intertidal zone. This species of hermit crab has been observed to be quite aggressive, therefore yielding staggering amounts of both intraspecific and interspecific competition. Smaller individuals have been recorded to be more aggressive and dominant, which may be the result of an adaptation to accommodate for smaller size. [11]

Diet

The diet of these organisms, like many other species of hermit crab, includes macroscopic animals and detritus, due to the fact that hermit crabs are classified as omnivorous detritivores. In addition, the bulk of their nutrient intake comes from detritus, classified by many marine scientists as “marine snow”. They consume their food sources through proteolytic enzymes that split carbohydrates and lipids. [12]

Threats

Some of the threats to this species include a microbial infection, which is the result of the fungus Fusarium solani . This fungus causes lesions, attack of the dermis, and mixed inflammatory response, therefore reducing the organism's ability to fight off infection. [13] In addition, larval parasitic nematodes, such as Hysterothylacium aduncum, have been reported to infect this species of hermit crab and hosts itself as a parasite within the individual. One to three of these parasitic nematodes were observed per hermit crab by David J. Marcogliese during his study of nematodes of the past of Eastern Canada, and defined Hysterothylacium aduncum as intestinal parasites. [14] Though not much is known on their affect to the organisms with which they inhabit, their position within the gut of their host may be in order to consume the food that the organism has ingested, causing possible starvation to the host. A common invasive species affecting Pagurus acadianus is the Asian shore crab, Hermigraspus sanguineus , which outcompetes many different species of crab as a result of being aggressive interspecific competitors. [15] The introduction of this invasive species was first observed in New Jersey in 1988. In their work, Christopher P. Bloch, Kevin D. Curry, and John C. Jahoda attribute their occurrence to international commerce and global travel. [16]

Defenses

Acadian hermit crabs have been cited to have two major defense mechanisms: fleeing when approached in the face of predation, or curling up and hiding in their shells. They decide which tactic to use depending on cost–benefit analysis. Like many terrestrial and marine organisms alike, Pagurus acadianus will choose either method depending on the exhaustion of energy or the depleted availability of food during a threat. [17]

Related Research Articles

<span class="mw-page-title-main">Ectosymbiosis</span> Symbiosis in which the symbiont lives on the body surface of the host

Ectosymbiosis is a form of symbiotic behavior in which an organism lives on the body surface of another organism, including internal surfaces such as the lining of the digestive tube and the ducts of glands. The ectosymbiotic species, or ectosymbiont, is generally an immobile organism existing off of biotic substrate through mutualism, commensalism, or parasitism. Ectosymbiosis is found throughout a diverse array of environments and in many different species.

<span class="mw-page-title-main">Crab</span> Infraorder of decapod crustaceans

Crabs are decapod crustaceans of the infraorder Brachyura, which typically have a very short projecting "tail" (abdomen), usually hidden entirely under the thorax. They live in all the world's oceans, in freshwater, and on land, are generally covered with a thick exoskeleton, and have a single pair of pincers. They first appeared during the Jurassic Period.

<span class="mw-page-title-main">Hermit crab</span> Superfamily of crustaceans (Paguroidea)

Hermit crabs are anomuran decapod crustaceans of the superfamily Paguroidea that have adapted to occupy empty scavenged mollusc shells to protect their fragile exoskeletons. There are over 800 species of hermit crab, most of which possess an asymmetric abdomen concealed by a snug-fitting shell. Hermit crabs' soft (non-calcified) abdominal exoskeleton means they must occupy shelter produced by other organisms or risk being defenseless.

<span class="mw-page-title-main">Tide pool</span> Rocky pool on a seashore, separated from the sea at low tide, filled with seawater

A tide pool or rock pool is a shallow pool of seawater that forms on the rocky intertidal shore. These pools typically range from a few inches to a few feet deep and a few feet across. Many of these pools exist as separate bodies of water only at low tide, as seawater gets trapped when the tide recedes. Tides are caused by the gravitational pull of the sun and moon. A tidal cycle is usually about 25 hours and consists of one or two high tides and two low tides.

<i>Pagurus bernhardus</i> Species of crustacean

Pagurus bernhardus is the common marine hermit crab of Europe's Atlantic coasts. It is sometimes referred to as the common hermit crab or soldier crab. Its carapace reaches 3.5 centimetres (1.4 in) long, and is found in both rocky and sandy areas, from the Arctic waters of Iceland, Svalbard and Russia as far south as southern Portugal, but its range does not extend as far as the Mediterranean Sea. It can be found in pools on the upper shore and at the mean tide level down to a depth of approximately 140 metres (460 ft), with smaller specimens generally found in rock pools around the middle shore and lower shore regions, with larger individuals at depth. P. bernhardus is an omnivorous detritivore that opportunistically scavenges for carrion, and which can also filter feed when necessary.

<i>Coenobita cavipes</i> Species of crustacean

Coenobita cavipes is a species of land hermit crab native to the eastern parts of Africa, the Indonesia, Philippines, China, Japan, Malaysia, Taiwan, Polynesia, and Micronesia. While these hermit crabs are terrestrial, they prefer to reside near the shores for access of both water and land.

<span class="mw-page-title-main">Jonah crab</span> Species of crab

The Jonah crab is a marine brachyuran crab that inhabits waters along the east coast of North America from Newfoundland to Florida. Jonah crabs possess a rounded, rough-edged carapace with small light spots, and robust claws with dark brown-black tips. The maximum reported carapace width for males is 222 mm, while females rarely exceed 150 mm. It is the closest relative to the European brown crab in the Western Atlantic.

<i>Pagurus longicarpus</i> Species of crustacean

Pagurus longicarpus, the long-wristed hermit crab, is a common hermit crab found along the Atlantic and Gulf coasts of the United States and the Atlantic coast of Canada.

<i>Pagurus novizealandiae</i> Species of crustacean

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<span class="mw-page-title-main">Epibiont</span> Organism that lives on surface of another living organism

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<i>Pagurus hirsutiusculus</i> Species of crustacean

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<span class="mw-page-title-main">Crustacean larva</span> Crustacean larval and immature stages between hatching and adult form

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Calcinus tubularis is a species of hermit crab. It is found in the Mediterranean Sea and around islands in the Atlantic Ocean, where it lives below the intertidal zone. Its carapace, eyestalks and claws are marked with numerous red spots. C. tubularis and its sister species, C. verrilli, are the only hermit crabs known to show sexual dimorphism in shell choice, with males using normal marine gastropod shells, while females use shells of gastropods in the family Vermetidae, which are attached to rocks or other hard substrates.

<i>Pagurus prideaux</i> Species of crustacean

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<i>Neanthes fucata</i> Species of annelid worm

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<i>Pagurus dalli</i> Species of crustacean

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References

  1. 1 2 "Pagurus acadianus Report". Integrated Taxonomic Information System. Retrieved 2018-05-04.
  2. "Pagurus acadianus species details". Catalogue of Life. Retrieved 2018-05-04.
  3. "Pagurus acadianus". GBIF. Retrieved 2018-05-04.
  4. "Pagurus acadianus Species Information". BugGuide.net. Retrieved 2018-05-04.
  5. 1 2 "Acadian hermit crab (Pagurus acadianus)". iNaturalist.org. Retrieved 2019-03-22.
  6. 1 2 Grant, William C. (1963). "Notes on the Ecology and Behavior of the Hermit Crab, Pagurus acadianus". Ecology. 44 (4): 767–771. doi:10.2307/1933025. ISSN   0012-9658. JSTOR   1933025.
  7. 1 2 Roberts, Morris H. (1973). "Larval Development of Pagurus acadianus Benedict, 1901, Reared in the Laboratory (Decapoda, Anomura)". Crustaceana. 24 (3): 303–317. doi:10.1163/156854073X00669. ISSN   0011-216X. JSTOR   20101991.
  8. "Aquatic Biodiversity Monitoring Network". www.rsba.ca. Retrieved 2019-03-22.
  9. "Pagurus acadianus J.E.Benedict, 1901". www.gbif.org. Retrieved 2019-03-22.
  10. Angel, Jennifer E. (January 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.
  11. Grant, William C.; Ulmer, Kevin M. (1974-02-01). "Shell selection and aggressive behavior in two sympatric species of hermit crabs". The Biological Bulletin. 146 (1): 32–43. doi:10.2307/1540395. ISSN   0006-3185. JSTOR   1540395. PMID   4856150.
  12. Hazlett, B A (1981). "The Behavioral Ecology of Hermit Crabs". Annual Review of Ecology and Systematics. 12 (1): 1–22. doi:10.1146/annurev.es.12.110181.000245.
  13. Smolowitz, R. M.; Bullis, R. A.; Abt, D. A. (1992). "Mycotic Branchitis in Laboratory-Maintained Hermit Crabs (Pagurus spp.)". Journal of Crustacean Biology. 12 (2): 161–168. doi:10.2307/1549070. ISSN   0278-0372. JSTOR   1549070.
  14. Marcogliese, David J. "Larval Parasitic Nematodes Infecting Marine Crustaceans in Eastern Canada. 3. Hysterothylacium aduncum" (PDF). Bionames.
  15. Westgate, Kimberly (2011-01-01). "The Invasive Asian Shore Crab, a Dominant Species on Southeastern Massachusetts Beaches: A Cause for Concern". Undergraduate Review. 7 (1): 131–137.
  16. Jahoda, John C.; Curry, Kevin D.; Bloch, Christopher P. (March 2015). "Long-Term Effects of an Invasive Shore Crab on Cape Cod, Massachusetts". Northeastern Naturalist. 22 (1): 178–191. doi:10.1656/045.022.0118. ISSN   1092-6194. S2CID   54044491.
  17. Scarratt, Alison M.; Godin, Jean-Guy J. (1992-04-28). "Foraging and antipredator decisions in the hermit crab Pagurus acadianus (Benedict)". Journal of Experimental Marine Biology and Ecology. 156 (2): 225–238. doi:10.1016/0022-0981(92)90248-9.

Further reading