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Neotrypaea californiensis
bay ghost shrimp


By Stephanie Astle; Victoria Hosford; Dennis Ramirez

Kingdom: Animalia
Class: Malacostraca
Order: Decapoda
Family: Callianassidae
Genus: Neotrypaea
Species: Neotrypaea californiensis

Geographic Range

Neotrypaea californiensis can be found at intertidal locations within the regions of the North American West Coast ranging from Mutiny Bay, Alaska to Tijuana River, San Diego County, California and El Estuario de Punto Banda, Baja California Norte, Mexico. (MacGinitie, 1934; Ricketts and Calvin, 1968)

Biogeographic Regions
nearctic (Native ); pacific ocean (Native )

Habitat

Range depth
0.76 (low) m
(2.49 (low) ft)

Neotrypaea californiensis live as infauna in intertidal areas between the middle to low intertidal zones, on sandy beaches or tidal flats in estuaries. Ghost shrimp habitat is distinguished by numerous holes that are the entrances and exits of their burrows. Ghost shrimp are constantly excavating complex tunnels under the sand. (MacGinitie, 1934)

Although the majority of time is spent building tunnels, ghost shrimp do come to the surface at times, where predation can occur. (Posey, 1985)

Habitat Regions
saltwater or marine

Aquatic Biomes
benthic ; coastal

Wetlands
marsh

Other Habitat Features
estuarine ; intertidal or littoral

Physical Description

Average mass
1-5 g
( oz)

Average length
10-12 cm
( in)

Body coloration ranges between shades of orange, pink, and red. Some individuals may also exhibit a very pale coloration, almost white. The main body parts of Neotrypaea californiensis follow a generalized decapod body plan: two differently-shaped claws (with one major cheliped, often several times larger than the opposite claw); five pairs of legs, three paddle-shaped swimming legs (pleopods), a fan-like tail (uropod), telson, flattened eyestalks, and two pairs of antennae. The exoskeleton is fringed with numerous fine hairs. (MacGinitie, 1934)

Females bearing eggs carry them on their abdomen. The egg mass may vary in color between individuals, from light yellow to deep scarlet. The major cheliped is sexually dimorphic, being larger on males. The major cheliped can account for up to a quarter of a ghost shrimp's weight. (Labadie and Palmer, 1996)

Other Physical Features
ectothermic ; heterothermic ; bilateral symmetry

Sexual Dimorphism
male larger; sexes shaped differently

Development

Neotrypaea californiensis matures between 18 and 24 months. Mature individuals can be found closest to the ocean and they grow much faster compared to individuals located nearer to shore. Larger sized females with larger eggs can be found within intertidal areas.

Females carry their fertile eggs on their abdomen and the eggs are released in June or July. The newly released ghost shrimp larvae (zoea) drift for six to eight weeks in the water column as zooplankton, passing through five zoeal stages before transforming into a megalops. There zoeal stages take place over 6 to 8 weeks. They will return to estuarine habitats as megalopae on flood tides during August. (Bird, 1982; MacGinitie, 1934; McCrow, L.T., 1972)

Reproduction

Using olfactory receptors on their antennules called aesthetascs, a male ghost shrimp detects water soluble substances released by premolt females. Once a female is found, the male will follow and protect her from predators and other suitors with his major cheliped, until she molts. This process is known as temporary mate guarding. After the female molts, the male mates with her and then leaves her to find another premolt female. (Bauer, 2011; Labadie and Palmer, 1996)

Mating System
polygynandrous (promiscuous)

Breeding interval
April to August

Breeding season
Begins in April

Range number of offspring
200 to 1,400

Range gestation period
3 to 5 months

Average birth mass
0.62-mm diameter at extrusion to 0.83 mm when eyed g
( oz)

Average time to independence
Eggs are carried and protected by the female for 3- 5 months before hatching, releasing larvae into the water column as plankton months

Average age at sexual or reproductive maturity (female)
18-24 months months

Average age at sexual or reproductive maturity (male)
18-24 months months

Though the mating behavior of the ghost shrimp is largely unknown, it is agreed that the males use the major cheliped to fight other males for reproductive access to females.

The female will carry her brood of eggs for approximately 3 to 5 months. Hatching occurs in June or July. The newly released ghost shrimp larvae (zoea) drift for six to eight weeks in the water column as zooplankton, passing through five zoeal stages before transforming into a megalops. They will return to estuarine habitats as megalopae on flood tides during August. (Horning, et al., 1989; Labadie and Palmer, 1996)

Key Reproductive Features
seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization (Internal ); oviparous

Ghost shrimp reproduce seasonally. The female will carry her brood of eggs for approximately 3 to 5 months until they hatch, usually in June or July. (Horning, et al., 1989)

Parental Investment
precocial ; female parental care ; pre-hatching/birth (Protecting: Female)

Lifespan/Longevity

Average lifespan
Status: wild

5 years

Average lifespan
Status: wild

3-5 years

Ghost shrimp in the wild have an average lifespan of 3-5 years. The primary factor affecting lifespan is the level of available nutrients. Nutrient availability is directly related to the distance of the colony to an estuary. Longer-lived shrimp are found closer the mouth of an estuary. (Bird, 1982; Dumbauld, et al., 1996)

Behavior

Water temperature and substrate characteristics can also influence shrimp activities, as colder temperatures reduce shrimp mobility and sandy sediments reduce its ability to burrow.

Ghost shrimp in general are constantly burrowing to obtain food. (Horning, et al., 1989; Pernet, B., Deconinck, A., and Haney, L, 2010; Wicksten, 2008)

Key Behaviors
motile ; sedentary ; solitary

Home Range

Ghost shrimp conduct their daily activities within a relatively small circumscribed area. Under experimental conditions, ghost shrimp spent over 25% of the time within 2 cm of the burrow entrance; furthermore, the shrimp were also observed to move from one burrow to another. (Posey, 1985; Wicksten, 2008)

Ghost shrimp territory is limited to a few cm within the vicinity of their own burrow, which they defend from rivals. Population size can be very dense with burrows directly adjacent to those of conspecifics. In Oregon, densities have been estimated at 700-1,400 per square meter in Yaquina bay; 420-770 per square meter in Sand Lake Estuary, and less than 300 per square meter along the coast. (Bird, 1982; McCrow, L.T., 1972)

Communication and Perception

Tactile: This species uses its antennae, chelipeds, and sensory hairs (called cuticular mechanoreceptors, covering most of the body) to sense physical objects in the environment.

Vision: Eyestalks are acute with divergent tips, and bear a pigmented cornea in the middle of the eyestalk. (Nau, 2004)

Communication Channels
visual ; tactile ; chemical

Perception Channels
visual ; tactile ; chemical

Food Habits

Ghost shrimp ingest plankton and detritus deposits scraped from the sediments during burrowing. Plankton is also obtained as water and detrital materials pass over the body and are collected on the hairs of their second and third walking legs. (Nau, 2004)

To find enough food, ghost shrimp tunnel almost constantly, reworking the sediment to a depth of as much as 76 cm. (Horning, et al., 1989)

Primary Diet
planktivore ; detritivore

Animal Foods
aquatic or marine worms; zooplankton

Plant Foods
phytoplankton

Other Foods
detritus

Foraging Behavior
filter-feeding

Predation

Known Predators


Although ghost shrimp typically inhabit deep burrows, they are susceptible to predation because they sometimes venture outside of their burrow entrances. Fishes and invertebrates are significant predators when the tide is high, whereas shorebirds and humans prey on ghost shrimp when the tide is low. Shorebirds that feed on ghost shrimp include the long-billed curlew Numenius americanus and the willet Catoptrophorus semipalmatus. Some fish predators include the Pacific staghorn sculpin, Leptocottus armatus. (Light, S., Carlton, T, 2007; Posey, 1985; Posey, M. H, 1986; Stenzel, L., Huber, H., and Page, P, 1976)

Ecosystem Roles

The vigorous burrowing activities of ghost shrimp have such dramatic effects on their habitats of soft sediment that these animals are often considered ecosystem engineers. By aerating the surface sediment through burrowing, the ghost shrimp provide an environment attractive to other species including the blind goby, three species of pea crabs, two species of clams, a copepod, a shrimp, polynoid worms, and isopods, all of which live within the burrows. (Horning, et al., 1989; Pernet, B., Deconinck, A., and Haney, L, 2010)

Ecosystem Impact
creates habitat; soil aeration

Commensal/Parasitic Species

Economic Importance for Humans: Positive

Neotrypaea californiensis is used as live bait by fishermen. Fishermen commonly call them one-armed bandits because of their one long cheliped. (Nau, 2004)

Positive Impacts
food

Economic Importance for Humans: Negative

No known negative economic importance for humans.

Conservation Status

IUCN Red List of Threatened Species [Link]
Not Evaluated.

US Federal List [Link]
No special status

CITES [Link]
No special status

State of Michigan List [Link]
No special status

Other Comments

Neotrypaea californiensis is tolerant of low oxygen conditions, and laboratory results indicate this species can survive anoxic conditions for as long as 3 days. (Thompson and Pritchard, 1969)

For More Information

Find Neotrypaea californiensis information at

Contributors

Stephanie Astle (author), Mesa College of San Diego, Victoria Hosford (author), Mesa College of San Diego, Dennis Ramirez (author), Mesa College of San Diego, Paul Detwiler (editor), Mesa College of San Diego, Renee Mulcrone (editor), Special Projects, Alexa Unruh (editor), University of Michigan.

References

Bauer, R. 2011. Chemical Communication in Crustaceans. New York: Springer. Accessed June 21, 2011 at http://www.springerlink.com/content/l6177qk20255t215/.

Bird, E. 1982. Population dynamics of thalassinidean shrimps and community effects through sediment modification. Ph.D. Dissertation. University of Maryland, College Park: 1-151.

Dumbauld, B., D. Armstrong, K. Feldman. 1996. Life history characteristics of two sympatric thalassinidean shrimps, Neotrypaea californiensis and Upogebia pugettensis, with implications for oyster culture. Journal of Crustacean Biology, 16(4): 689-708.

Horning, S., A. Sterling, S. Smith. 1989. Species profiles: life histories and environmental requirements of coastal fishes and invertebrates (Pacific Northwest)--ghost shrimp and blue mud shrimp. U.S. Fish Wildlife Service, Report No. TR EL-82-4: 1-15.

Labadie, L., A. Palmer. 1996. Pronounced heterochely in the ghost shrimp, Neotrypaea californiensis (Decapoda: Thalassinidea: Callianassidae): allometry, inferred function and development. Journal of Zoology, 240(4): 659-675.

Light, S., Carlton, T, 2007. The Light and Smith Manual: Intertidal Invertebrates from Central California to Oregon. ISBN 0520239393, 9780520239395: University of California Press.

MacGinitie, G. 1934. The natural history of Callianassa californiensis Dana. American Midland Naturalist, 15: 166-177.

MacGinitie, G. 1935. Ecological aspects of a California marine estuary. American Midland Naturalist, 16: 629-765.

MacGinitie, G., N. MacGinitie. 1968. Natural history of marine animals, 2nd ed.. New York: NcGraw-Hill.

McCrow, L.T., 1972. The ghost shrimp Callianassa californiesis Dana, 1854, in Yaquina Bay, Oregon. M.S. Thesis. Oregon State University, Corvallis: 56.

Morris, R., D. Abbott, E. Haderlie. 1980. Intertidal invertebrates of California. Stanford: Stanford University Press.

Nau, F. 2004. "Callianassa californiensis (Dana, 1854)" (On-line). Accessed June 20, 2011 at http://academic.evergreen.edu/curricular/invertebratezoology/webpage/californiensis/callianassacaliforniensis.htm.

Pernet, B., Deconinck, A., and Haney, L, 2010. Molecular morphological markers for distinguishing the sympatric intertidal ghost shrimp Neotrypaea californiensis and N. gigas in the Eastern Pacific. Journal of Crustacean Biology, 30 (2): 323-331.

Posey, M. H, 1986. Changes in a benthic community associated with dense beds of a burrowing deposit feeder Callianassa californiensis. Marine Ecology Progress Series, 31: 15-22.

Posey, M. 1986. Predation on a burrowing shrimp: distribution and community consequences. Journal of Experimental Marine Biology and Ecology, 103: 143 -161.

Posey, M. 1985. The effects upon the macrofaunal community of a dominant burrowing deposit feeder, Callianassa californienis, and the role of predation in determining its intertidal distrution. PhD Dissertation: 1-119.

Ricketts, E., J. Calvin. 1968. Low Intertidal. Pp. 237 in J Hedgpeth, ed. Between Pacific Tides. Stanford, CA: Stanford University Press.

Shimoda, K., Wardiatno, Y., Kubo K. and Tamaki, A, 2005. Intraspecific behaviors and major cheliped sexual dimorphism in three congeneric callianassid shrimp. Marine Biology, 146(3): 543-557.

Stenzel, L., Huber, H., and Page, P, 1976. Feeding behavior and diet of the long-billed curlew and willet. The Wilson Bulletin, 88(2): 314-332.

Thompson, R., A. Pritchard. 1969. Respiratory adaptations of two burrowing crustaceans, Callianassa californiensis and Upogebia pugettensis (Decapoda, Thalassinidea). Biological Bulletin, 136: 274-287.

Wicksten, M. 2008. Decapod Crustacea of the Californian and Oregonian Zoogeographic Provinces. Scripps Institution of Oceanography Library Paper, 26: 1-413. Accessed June 20, 2011 at http://escholarship.org/uc/item/7sk9t2dz.

To cite this page: Astle, S.; V. Hosford and D. Ramirez 2011. "Neotrypaea californiensis" (On-line), Animal Diversity Web. Accessed June 01, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Neotrypaea_californiensis.html

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.

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