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Pycnopodia helianthoides


By Shayna Yagoda

Kingdom: Animalia
Class: Asteroidea
Order: Forcipulatida
Family: Asteriidae
Genus: Pycnopodia
Species: Pycnopodia helianthoides

Geographic Range

Pycnopodia helianthoides is commonly found in marine environments ranging from the shallow waters of the Aleutian Islands, Alaska, to San Diego, California. (Lambert, 2000)

Biogeographic Regions
nearctic ; pacific ocean

Habitat

Range depth
435 (high) m
(1427.17 (high) ft)

Sunflower stars are commonly found on various substrates like mud, sand, gravel, boulders and rock. They are found from the intertidal zone to 435 m, however, most are found no more than 120 m. (Lambert, 2000)

Habitat Regions
temperate ; saltwater or marine

Aquatic Biomes
benthic

Other Habitat Features
intertidal or littoral

Physical Description

Pycnopodia helianthoides, the largest of the sea stars, is radially symmetrical. The sunflower star has more arms than any other species, numbering between 15 and 24 (most sea stars have between 5 and 14), and is the heaviest known sea star, weighing about 5 kg. Their arms are up to 40 cm long and they are usually around 80 cm in diameter. The colors vary. Some are reddish-orange to yellow, violet brown, purplish or slatey purple. The stomach is found on the underside of the center body, or the oral surface. This area is usually a lighter color with yellow or orange tube feet. Pycnopodia helianthoides has over 15,000 tube feet which have suction cups that allow the stars to cling to rocks. The suctions cups are so strong that if you try to pull a sea star of a rock, the suctions cups may break lose from the sea star and continue to stick on the rock. (Ahearn and Benhnke, 1991; Esquivel, 2003; Lambert, 2000; )

Other Physical Features
ectothermic ; heterothermic ; radial symmetry

Sexual Dimorphism
sexes alike

Development

The eggs develop into swimming, bilateral larvae that usually remain in the plankton for no more than 10 weeks. The larval form feeds on single-celled plants. When the larva settles on the bottom it metamorphoses into a young sea star with five arms. The young P. helianthoides initially feeds on the thin layer skin-celled plants that coat the bottom of their marine habitat. The juvenille soon adds an arm clockwise from the bivium. Additional arms are added bilaterally in pairs to either side of the sixth ray. Each new pair is inserted between the last pair formed and the adjacent original arms. (Alender, et al., 1966; Lambert, 2000)

Development - Life Cycle
metamorphosis

Reproduction

There is no sexual dimorphism within these species. Fertilization is external. (Lawrence, 1987)

Mating System
polygynandrous (promiscuous)

Breeding interval
Between March and July

Pycnopodia helianthoides breeds by broadcast fertilization between March and July. However, the main peak is May and June. Each separate sex sheds its eggs or sperm into the water where the fertilization takes place by chance. (Alender, et al., 1966; Lambert, 2000)

Key Reproductive Features
seasonal breeding ; sexual ; fertilization (External ); oviparous

There is no parental care within this species.

Parental Investment
pre-fertilization (Provisioning)

Lifespan/Longevity

Typical lifespan
Status: wild

3 to 5 years

Average lifespan
Status: wild

3-5 years

Sea stars have a life span usually between 3 and 5 years. ("Sea Stars", 2002)

Behavior

Pycnopodia helianthoides is solitary.

Sunflower star have the ability to regenerate its arms which may detach as a means of defense when handled excessively or attacked by a predator. A whole new sea star may form if the detached arm has a portion of the central disk is included.

Pycnopodia helianthoides primarily moves by walking on its tube feet which possess suckers. This particular sea star can move more rapidly because of its flexible body and the aboral skeletal plates are loosely connected to one another.

Pycnopodia helianthoides migrates up and down the shore with the tide and exhibits annual migration as well. (Alender, et al., 1966; Lambert, 2000)

Key Behaviors
motile ; migratory ; solitary

Communication and Perception

If a predator attacks, P. helianthoides can let its arm drop off and send a chemical that causes an alarm response to other sunflower stars in the area. If its arm is irritated or disturbed by a predator, it will drop it off or autotomize its arm. The autotomy is triggered by a chemical that is released by injured tissues. This allows sunflower stars to escape from the predator holding onto its arm. (Lambert, 2000)

Communication Channels
chemical

Other Communication Modes
pheromones

Perception Channels
visual ; tactile ; chemical

Food Habits

Pycnopodia helianthoides is primarily carnivorous, feeding on mussels, sea urchins, fish, crustaceans (crabs and barnacles), sea cucumbers, clams, gastropods, sand dollars, and occasionally algae and sponges. However, the diet varies with geographic location and the availability of prey. For example, on the west coast, studies show that sea urchins are its main prey. For most sunflower stars, sea urchins make up 21-98% of their diet. Sunflower stars use their strong sense of smell and very sensitive indicators of light and dark to find their prey, and can move at a quick rate of 10 cm per second or 18 feet per minute. While moving, it puts its leading 8 arms in front and when it contacts the prey, it throws the leading arms down on top of the prey. Pycnopodia helianthoides then protrudes its stomach, envelops the entire prey, and digests it. The arms and greatly expandable tube feet are the basic tools of prey capture. Many species have developed escape responses to sunflower stars. For example, the abalone Haliotis accelerates and at the same time whips it shell back and forth to break the grasp of the tube feet of the sea star. (Ahearn and Benhnke, 1991; Esquivel, 2003; Lambert, 2000; )

Animal Foods
mollusks; aquatic crustaceans; echinoderms; other marine invertebrates

Plant Foods
algae

Predation

Known Predators


Sea stars have very few predators, especially P. helianthoides. Sometimes Alaska king crab and sea otters may attack sea stars. Birds such as gulls have been known to prey upon sunflower stars. The magnitude of loss of intertidal P. helianthoides is enough to explain the near absence of these soft-bodied sea stars in the intertidal zone of Tatoosh. Pycnopodia helianthoides can have large subtidal populations that do not experience bird predation resulting in a little effect on their total population sizes. Predators mainly eat the sea stars during their larval and juvenile stages. The availability of food, rather than predation, limits the number of adult sunflower stars. (Lambert, 2000; Wootton, 1997)

Ecosystem Roles

Pycnopodia helianthoides regulates the structure of the benthic community. Between Oregon and the northern Gulf of Alaska, this abudant sea star is the only species considered to be an important sea urchin predator. Pycnopodia helianthoides coexists with its prey while otters decimate urchin populations; therefore, they have a more subtle effect. Pycnopodia helianthoides creates small-scale, prey-free patches by consuming few prey individuals, while the remaining prey exhibit a strong escape response. Since the urchins are herbivorous, the short-term existence of prey-free patches can influence plant diversity and community primary productivity. (Dayton, 1975; Duggins, 1983; )

Economic Importance for Humans: Positive

There was no information regarding the economic importance of P. helianthoides to humans.

Economic Importance for Humans: Negative

This species is viewed by many commercial fishers as a pest. The results of the sunflower star's predacious behavior fouls long-line gear and crab pots. (Holmes, 1994)

Conservation Status

IUCN Red List [Link]
Data Deficient

US Federal List [Link]
No special status

CITES [Link]
No special status

Other Comments

Pycnopodia helianthoides is one of the most interesting and unique sea stars in its class. It is one of the biggest, has the most arms, and also can move the fastest. Its radiant colors and shape are also unique. (Lambert, 2000; Lawrence, 1987; )

For More Information

Find Pycnopodia helianthoides information at

Contributors

Renee Sherman Mulcrone (editor), .

Shayna Yagoda (author), University of Michigan-Ann Arbor, Phil Myers (editor), Museum of Zoology, University of Michigan.

References

Tropica Beach. 2002. "Sea Stars" (On-line ). Accessed 03/25/03 at http://www.tropicabelize.com/Crab%20Collection/Crabs%20Photos/Sea%20Stars.htm.

Ahearn, G., R. Benhnke. 1991. Diet, Feeding-Behaviour, and Surface-Morphology of the Multiarmed Antartic Sea Star Labidiaster-Annulatus. Marine Ecology- Progress Series, 77/1: 65-84.

Alender, C., J. Anderson, J. Binyon, R. Boolootian, D. Davenport. 1966. Physiology of Echinodermata. New York: Interscience.

Dayton, P. 1975. Experimental Evaluation of Ecological Dominance in a Rocky Intertidal Algal Community. Ecological Monographs, 45/2: 137-159.

Duggins, D. 1983. Starfish Predation and the Creation of Mosaic Patterns in a Kelp-Dominated Community. Ecology, 64/6: 1610-1619.

Esquivel, C. 2003. "Critter Care Club-species list: Invertebrates" (On-line). Accessed December 08, 2004 at http://www.cabrilloaq.org/critter1.htm.

Holmes, P. 1994. "Star Fish" (On-line). Accessed December 09, 2004 at http://www.adfg.state.ak.us/pubs/notebook/shellfsh/starfish.php.

Lambert, P. 2000. Sea Stars of British Columbia, Southeast Alaska and Puget Sound. Vancouver: UBC Press.

Lawrence, J. 1987. A Functional Biology of Echinoderms. Baltimore: The John Hopkins University Press.

Wootton, J. T. 1997. Estimates and Tests of Per Capita Interaction Strength: Diet, Abundance, and Impact of Intertidially Foraging Birds. Ecological Monographs, 67/1: 45-64.

To cite this page: Yagoda, S. 2004. "Pycnopodia helianthoides" (On-line), Animal Diversity Web. Accessed February 12, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Pycnopodia_helianthoides.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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