Overview
Comprehensive Description
This species lives permanently below the euphotic zone. Although its water content increases in winter, suggesting fluctuations in food availability, its O:N ratio changes little indicating that its lipid levels remain high and it is not starving (Hiller-Adams and Childress, 1983). Both its metabolic rate and ammonia excretion decrease with starvation (Hiller-Adams and Childress 1983, Quetin et al., 1980).
Neognathophausia ingens swims primarily with the pleopods, with some participation by the thoracic exopods (Hessler, 1985). Their activity levels are little affected by pressure (Quetin and Childress, 1980). The species swims constantly and has a relatively high drag compared to fish (Cowles et al., 1985), but swims at a speed which minimizes energy losses due to drag (Cowles and Childress, 1988).
Gnathophausia means "light-jaw". This species has a gland on its second maxillae (mouthparts) from which it spews a brilliantly luminescent cloud into the water when disturbed. Luminescence seems to be a function of diet, since animals maintained on non-luminescent food in the laboratory gradually lose their ability to luminesce, while if luminescent food is restored they can regain their luminescence (Frank et al., 1984).
This species often lives in oxygen minimum layers, yet its metabolism is entirely aerobic (Childress 1968, 1969, 1971, Cowles et al., 1991). To facilitate oxygen diffusion, it maintains a high rate of oxygen flow over its gills and extracts a very high percentage of the available oxygen (Childress, 1971). Its low rate of aerobic metabolism (Childress, 1971, Cowles, 1987, Cowles et al., 1991) help keep it from building up oxygen debt. It has greater gill surface area than do most crustaceans and fishes (Belman and Childress, 1976). The oxygen diffusion distance across the gills is 1.5 to 2.5 microns, comparable to that found in many fishes (Belman and Childress, 1976). It maintains relatively high rates of blood flow via large circulatory system components. Its heart rate is similar to that of other similarly-sized crustaceans, and the heart slows as oxygen limitation is reached (Belman and Childress, 1976). It appears that much of the oxygen in the blood is carried by hemocyanin, which has a high oxygen affinity and cooperativity and a large Bohr shift (Sanders and Childress, 1990). Species which live in areas with very low oxygen levels, such as off California, are able to live aerobically at lower oxygen levels than are those from higher oxygen levels such as Hawaii (Cowles et al., 1991).
Predators include the Melanostominid fish Echiostoma barbatum (Sutton and Hopkins, 1996), the Macrourid fish Macrouronus novaezelandiae (Clark, 1985), dwarf sperm whale (Cardona-Maldonado and Mignucci-Giannoni (1999), the Antillean beaked whale (Debrot, 1998), in which it comprised 41% of the stomach contents of a beached individual, and Cuvier's beaked whale (Palacios, 2003).
The rostrum and spines of small individuals are relatively longer than in large individuals. This led to small individuals originally having been named a separate species, Gnathophausia calcarata.
Gnathophausia ingens is sometimes parasitized by an ellobiopsid flagellate protozoan, Amallocystis fascitus, which forms a cluster of white filaments on the ventral side of the anterior abdominal segment. The parasite seems to be associated with the main nerve ganglion in this segment, and is associated with hypertrophy of the ganglion. It also retards sexual maturation such as retarded development of oostegites in females and feminizing changes in males.
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Distribution
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van der Land, J.; Brattegard, T. (2001). Mysidacea, in: Costello, M.J. et al. (Ed.) (2001). European register of marine species: a check-list of the marine species in Europe and a bibliography of guides to their identification. Collection Patrimoines Naturels, 50: pp. 293-295
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1408
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Institute of Ocean Science Zooplankton Database
http://www.marinespecies.org/copepoda/aphia.php?p=sourcedetails&id=150286
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Tattersall, O.S. 1955. Mysidacea.-- Discovery Reports 28: 1-190, 46 figs.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=19162
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Mauchline, J. & M. Murano (1977) World list of the Mysidacea, Crustacea. - J. Tokyo Univ. Fish., 64 (1): 39-88
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=9412
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Sars, G.O. (1883). Preliminary notices on the Schizopoda of H.M.S. Challenger Expedition Forh. Videnskabsselsk. Kristiania 7: 1-43
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=9450
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Physical Description
Look Alikes
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Ecology
Habitat
Water temperature and chemistry ranges based on 66 samples.
Environmental ranges
Depth range (m): 0 - 3124
Temperature range (°C): 0.776 - 15.059
Nitrate (umol/L): 5.938 - 42.866
Salinity (PPS): 33.830 - 35.977
Oxygen (ml/l): 0.510 - 7.789
Phosphate (umol/l): 0.485 - 3.169
Silicate (umol/l): 2.685 - 120.197
Graphical representation
Depth range (m): 0 - 3124
Temperature range (°C): 0.776 - 15.059
Nitrate (umol/L): 5.938 - 42.866
Salinity (PPS): 33.830 - 35.977
Oxygen (ml/l): 0.510 - 7.789
Phosphate (umol/l): 0.485 - 3.169
Silicate (umol/l): 2.685 - 120.197
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Habitat: Bathypelagic
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Neognathophausia ingens
There is 1 barcode sequence available from BOLD and GenBank. Below is the sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species. See the BOLD taxonomy browser for more complete information about this specimen. Other sequences that do not yet meet barcode criteria may also be available.
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Download FASTA File
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Statistics of barcoding coverage: Neognathophausia ingens
Public Records: 7
Specimens with Barcodes: 7
Species With Barcodes: 1
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Wikipedia
Gnathophausia ingens
Gnathophausia ingens, the giant red mysid, is a species of lophogastrid crustacean with a pan-tropical distribution.[2] The adults may reach 350 millimetres (14 in) long, including the rostrum.[2] Females may brood their young for up to 530 days.[3] Brooding females live between 900 and 1,400 m (3,000 and 4,600 ft) in the eastern Pacific Ocean off California. They do not feed during this time.[4] When they feed, they prey on smaller crustaceans.[5]
References
- ^ a b Kenneth Meland & Jan Mees (2012). "Gnathophausia ingens (Dohrn, 1870)". In J. Mees & K. Meland. World List of Lophogastrida, Stygiomysida and Mysida. World Register of Marine Species. http://www.marinespecies.org/aphia.php?p=taxdetails&id=119929. Retrieved August 1, 2012.
- ^ a b Linda Haithcock Pequegnat (1965). "The bathypelagic mysid Gnathophausia (Crustacea) and its distribution in the eastern Pacific Ocean". Pacific Science 19 (4): 399–421. hdl:10125/7299.
- ^ J. J. Childress & M. H. Price (1978). "Growth rate of the bathypelagic crustacean Gnathophausia ingens (Mysidacea: Lophogastridae). I. Dimensional growth and population structure". Marine Biology 50 (1): 47–62. doi:10.1007/BF00390541.
- ^ J. J. Childress & M. H. Price (1983). "Growth rate of the bathypelagic crustacean Gnathophausia ingens (Mysidacea: Lophogastridae) II. Accumulation of material and energy". Marine Biology 76 (2): 165–177. doi:10.1007/BF00392733/.
- ^ "Giant red mysid". Monterey Bay Aquarium. http://www.montereybayaquarium.org/animals/AnimalDetails.aspx?enc=Z5SIVkZ+n+XOmL/K7IUhGw==. Retrieved 1 August 2012.
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