User:Reidtosa/Phronima sedentaria
Phronima sedentaria is a species of amphipod crustaceans found in oceans at a depth of up to 1 km (0.6 mi). They are large in size relative to other members of the genus Phronimidae.[1] Individuals may be found inside barrel-like homes, created most commonly from the outer layer, or tunic, of select species of tunicate, where they rear their young.[2] P. sedentaria is known to employ multiple feeding strategies and other interesting behaviors, including daily vertical migration.[2][3] The species is also known by the more common names “pram bug” and “barrel shrimp.”
Description
[edit]P. sedentaria is the largest and most abundant species in the family Phronimidae.[1][2] Sexual dimorphism is reflected between male and female members in the more extended and prominent antennae of the males relative to the short, reduced ones of females. More obviously, the size discrepancy between males and females distinguishes them further. Females measure up to 42 mm (1.7 in) long, while males are only 15 mm (0.6 in) long.[4] This species also possesses a complex optical system which involves the use of two sets of compound eyes.[2] Both sets use bundles of crystalline cones to process visual information: one set faces ventrally and one set faces dorsally.[2]
Ecology
[edit]![](http://upload.wikimedia.org/wikipedia/commons/thumb/c/c2/Salp_Barrel.jpg/236px-Salp_Barrel.jpg)
P. sedentaria most commonly exhibits a symbiotic relationship with tunicates of the genera Pyrosoma, Doliolum, and Salpa.[5] Females of P. sedentaria live in the barrel-like bodies of salps, pyrosomes, and cnidarians,[1] and use their strong pleopods to propel their homes through the water. They can somersault quickly in their barrels and thus change directions. However, speed is reduced by a factor of three to four when swimming while inside a barrel compared to swimming without one.[6] The shape of the barrel is generally asymmetrical, with one opening three times larger than that of the other.[6] It is not entirely certain how to classify the symbiotic relationship between P. sedentaria and its hosts, as instances of commensalism, parasitism, and predation have all been observed. However, some research has suggested that the majority of suborder Hyperiidea members exhibit parasitic behavior.[7][8][9] Females will locate a suitable salp, pyrosome, or cnidarian host and either cut into the host or enter through an existing opening. Once inside, the female will begin to consume the organism within and carve out the gelatinous inside, leaving nothing but the tunic. The cells on the tunic layer may serve various functions for the P. sedentaria, including protection from UV light, storage of acid, and defense against microorganisms, like bacteria.[10] In laboratory experiments with restricted access to potential hosts, females have additionally displayed competition for barrels.[2]
While certain prey (salps, pyrosomes, and cnidaria) have additional uses for P. sedentaria in hosting their young and providing feeding platforms, the species is also carnivorous on zooplankton, krill, arrowworms, other crustaceans, and other chaetognaths.[2][11] P. sedentaria use different feeding techniques depending on the food source, but the leading sets of pereiopods are primarily used in all cases. Mouth pieces, such as the mandible, maxillipeds, and maxillae, manipulate the food into small pieces which are then able to fit through the esophagus.[2] Feeding preferentially occurs at nighttime when members of this species undergo a vertical migration of around 200-350 meters to the ocean's surface.[3] Research has shown this species is susceptible to temperature fluctuations outside of the range 8-25 degrees Celsius (46-77 degrees Fahrenheit), which explains the desire for cooler deep water throughout the day and warmer shallow waters at night.[3] P. sedentaria typically migrate to hypoxic areas (such as the Oxygen Minimum Zone) during the day, causing low metabolic rates and physical activity.[12]
Known predators of P. sedentaria include the longnose lancetfish,[13] European flying squid,[14] Pacific pomfret,[15] albacore,[16] and skipjack tuna.[16]
Life Cycle & Development
[edit]Female P. sedentaria are capable of producing up to 600 eggs at a time.[16] The juveniles will spend their early early development within the mother in a specialized pouch called the marsupium. After finding a suitable host, the female will begin to transform the barrel into a nursery for its young. The female uses its pleopods to remove its offspring from a marsupium, while its pereiopods maintain stability and grasp onto the barrel.[2] Once inside, the young will organize themselves into a medial ring around the interior of the barrel. This shape is maintained until the mother delivers food, in which case the offspring will feed and return to formation afterward.[2] Young P. sedentaria will use the barrel as another food source. The offspring of Phronima sedentaria develop within their barrel homes until reaching prematurity, after which they are able to feed and survive independently.[1] Development is characterized by growth stages in which molting occurs.[1] Each molt adds a new segment to the rear sets of pleopods. The emergence of sexual dimorphism occurs soon after prematurity.[1]
- ^ a b c d e f Aoki, Masakazu N.; Matsumoto-Ohshima, Chie; Hirose, Euichi; Nishikawa, Jun (2013-04-23). "Mother–young cohabitation in Phronimella elongata and Phronima spp. (Amphipoda, Hyperiidea, Phronimidae)". Journal of the Marine Biological Association of the United Kingdom. 93 (6): 1553–1556. doi:10.1017/s0025315413000143. ISSN 0025-3154.
- ^ a b c d e f g h i j Diebel, Carol E. (1988-01-01). "OBSERVATIONS ON THE ANATOMY AND BEHAVIOR OF PHRONIMA SEDENTARIA (FORSKAL) (AMPHIPODA: HYPERIIDEA)". Journal of Crustacean Biology. 8 (1): 79–90. doi:10.1163/193724088x00107. ISSN 0278-0372.
- ^ a b c Elder, Leanne E.; Seibel, Brad A. (2015-09). "The thermal stress response to diel vertical migration in the hyperiid amphipod Phronima sedentaria". Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology. 187: 20–26. doi:10.1016/j.cbpa.2015.04.008. ISSN 1095-6433.
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(help) - ^ "Marine Species Identification Portal : Phronima sedentaria". species-identification.org. Retrieved 2021-03-20.
- ^ Ball, Eldon E. (1977-01). "Fine structure of the compound eyes of the midwater amphipod Phronima in relation to behavior and habitat". Tissue and Cell. 9 (3): 521–536. doi:10.1016/0040-8166(77)90010-6. ISSN 0040-8166.
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(help) - ^ a b Davenport, J. (1994-08). "Observations on the locomotion and buoyancy of Phronima sedentaria(Forskål, 1775) (Crustacea: Amphipoda: Hyperiidea)". Journal of Natural History. 28 (4): 787–793. doi:10.1080/00222939400770401. ISSN 0022-2933.
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(help) - ^ Madin, L.P.; Harbison, G.R. (1977-05). "The associations of Amphipoda Hyperiidea with gelatinous zooplankton—I. Associations with Salpidae". Deep Sea Research. 24 (5): 449–463. doi:10.1016/0146-6291(77)90483-0. ISSN 0146-6291.
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(help) - ^ Harbison, G.R.; Biggs, D.C.; Madin, L.P. (1977-05). "The associations of Amphipoda Hyperiidea with gelatinous zooplankton—II. Associations with Cnidaria, Ctenophora and Radiolaria". Deep Sea Research. 24 (5): 465–488. doi:10.1016/0146-6291(77)90484-2. ISSN 0146-6291.
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(help) - ^ Laval, Philippe (1978-01). "The barrel of the pelagic amphipod Phronima sedentaria (Forsk.) (Crustacea: hyperiidea)". Journal of Experimental Marine Biology and Ecology. 33 (3): 187–211. doi:10.1016/0022-0981(78)90008-4. ISSN 0022-0981.
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(help) - ^ Hirose, Euichi; Aoki, Masakazu N.; Nishikawa, Jun (2005-11-09). "Still alive? Fine structure of the barrels made by Phronima (Crustacea: Amphipoda)". Journal of the Marine Biological Association of the United Kingdom. 85 (6): 1435–1439. doi:10.1017/s0025315405012610. ISSN 0025-3154.
- ^ "Grzimek's animal life encyclopedia". Choice Reviews Online. 42 (01): 42–0029-42-0029. 2004-09-01. doi:10.5860/choice.42-0029. ISSN 0009-4978.
- ^ Elder, Leanne E.; Seibel, Brad A. (2015-09). "Ecophysiological implications of vertical migration into oxygen minimum zones for the hyperiid amphipod Phronima sedentaria". Journal of Plankton Research. 37 (5): 897–911. doi:10.1093/plankt/fbv066. ISSN 0142-7873.
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(help) - ^ Choy, CA; Portner, E; Iwane, M; Drazen, JC (2013-10-31). "Diets of five important predatory mesopelagic fishes of the central North Pacific". Marine Ecology Progress Series. 492: 169–184. doi:10.3354/meps10518. ISSN 0171-8630.
- ^ Rosas-Luis, Rigoberto; Villanueva, Roger; Sánchez, Pilar (2014-04). "Trophic habits of the Ommastrephid squid Illex coindetii and Todarodes sagittatus in the northwestern Mediterranean Sea". Fisheries Research. 152: 21–28. doi:10.1016/j.fishres.2013.10.009. ISSN 0165-7836.
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(help) - ^ WATANABE, HIKARU; KUBODERA, TSUNEMI; Kawahara, SHIGEYUKI (2003-04). "Feeding habits of Pacific pomfret Brama japonica inthe transition zone of the central North Pacific". Fisheries Science. 69 (2): 269–276. doi:10.1046/j.1444-2906.2003.00617.x. ISSN 0919-9268.
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(help) - ^ a b c Ball, Eldon E. (1977-01). "Fine structure of the compound eyes of the midwater amphipod Phronima in relation to behavior and habitat". Tissue and Cell. 9 (3): 521–536. doi:10.1016/0040-8166(77)90010-6. ISSN 0040-8166.
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: Check date values in:|date=
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