dcsimg

Description

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Body clear and colorless, sometimes opaque. Sometimes a pale red spot is present at the base of A1. Eye bright red.

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Diagnostic Description

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Posterior corners of the thorax are rounded, head smoothly rounded from side view. Caudal rami equal in length the anal segment, abdomen 1.5 times shorter than the cephalothorax. P5 four-segmented, the distal segment of P5 with 3 apical chaetae. A1 longer than the cephalothorax, but shorter than the body.

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Distribution

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Arctic and sub-Arctic, North Atlantic. On the Pacific side reaches the south of the Chukchi sea, is found near the coast of Alaska. In some areas are among the dominating species by abundance and biomass.

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Habitat

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Oceanic, epi- to bathypelagic species. Very well pronounced vertical migrations. Males dwell deeper than females.

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Morphology

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Female:
The back is only slightly arched. The posterior corners of the last thoracic segment are pulled back, rounded from side view. The genital segment is somewhat shorter than the combined length of the next 2 segments. Caudal rami short, equal in length to the anal segment. Abdomen 1.5 times shorter than the cephalothorax. A1 reach the middle of the middle of the genital segment. P5 four-segmented, the distal segment in thinner than the previous and carries 3 apical chaetae, of which the middle one is the longest. The distal edge of the 2nd and 3rd segments carries a spine facing the outside.

Male:
Body more slender and narrow than in female. The left (rarely right) A1 is geniculate. The distal segments of P5 elongate; a projection is present only on the right leg, the left leg does not carry spines or projections.

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Reproduction

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Egg-broadcasting species

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Size

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Female: 1,64-4,50 mm
Male: 1,59-4,00 mm

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Trophic Strategy

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Omnivorous; may feed on phytoplankton, microzooplankton and detritus.

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Metridia longa

provided by wikipedia EN

Metridia longa is a copepod found in the Arctic, the north Atlantic, the Pacific, and surrounding waters. The female has an average length of about 4.2 millimetres (0.17 in), and the males have an average length of about 3.5 millimetres (0.14 in).

Description

M. longa females have an average length of about 4.2 millimetres (0.17 in), with an average range between about 1.6 millimetres (0.063 in) and 4.5 millimetres (0.18 in). Males are usually smaller, with an average length of around 3.5 millimetres (0.14 in), and a range between about 1.6 and 4 millimetres (0.063 and 0.157 in).[1] M. longa are bioluminescent, emitting light when mechanically,[2] electrically, or chemically disturbed. This light is given through secretions containing luciferase from epidermal glands on the head and abdomen.[3]

Distribution

M. longa is found in the sub-Arctic, Arctic, north Atlantic, and the Pacific, along the coast of the Americas and Asia.[4] It has also been recorded in the Antarctic, in the Pacific Antarctic.[1]

Ecology

Life history and reproduction

At least in Balsfjorden, M. longa breeds from early to mid-May.[5] It uses recently ingested food to complete and release the eggs, but it likely uses stored lipids in oogenesis.[2] It has an average clutch size of about 33 eggs, not accounting for cannibalism. These eggs hatch with about 51% success after their 24-hour incubation period.[6] Stage I through V copepodites then develop during the summer.[5] Stages I through III are usually found below about 130 metres (430 ft) during the day, and generally do not migrate. In Arctic waters, it is typically found closer to the surface.[7] Also, in Balsfjorden, copepodite stages I through III were found to occur mostly in the top 50 metres (160 ft) of the fjord.[5] Copepodite stages IV through to the adult stage are migratory, moving from the deeper waters it inhabits during the day to shallower waters at night to feed. This is hypothesized to be because it could reduce the chance of predation, as predators relying on sight would find it harder to detect their prey in the dark.[7] This is further supported by the fact that it spends more time at the surface during the winter, when the nights are longer.[8] It is likely active during this winter season.[5] It also uses stored lipids to develop its gonads when it is overwintering.[2]

Feeding

M. longa is an omnivorous filter-feeder.[9] It cannibalizes its eggs, with a 2008 study finding it removed 38% of its eggs when food was abundant, until chlorophyll a concentrations reached below 50 milligrams (0.00011 lb) per 1 square metre (11 sq ft), when it started to remove an increasing amount of eggs, with a maximum of 85% of eggs removed.[6] It has been suggested that it uses omnivory during the winter to supplement its metabolic needs and its gonad development.[2]

References

  1. ^ a b Razouls C.; de Bovée F.; Kouwenberg J.; Desreumaux N. (2018). "Diversity and Geographic Distribution of Marine Planktonic Copepods". Sorbonne Université, CNRS. Retrieved 12 July 2018.
  2. ^ a b c d Buskey, Edward J.; Stearns, Donald E. (1991). "The effects of starvation on bioluminescence potential and egg release of the copepod Metridia longa". Journal of Plankton Research. 13 (4): 885–893. doi:10.1093/plankt/13.4.885.
  3. ^ Markova, Svetlana V.; Golz, Stefan; Frank, Ludmila A.; Kalthof, Bernd; Vysotski, Eugene S. (2004). "Cloning and expression of cDNA for a luciferase from the marine copepod Metridia longa". Journal of Biological Chemistry. 279 (5): 3212–3217. doi:10.1074/jbc.M309639200. PMID 14583604.
  4. ^ "Metridia longa" at the Encyclopedia of Life
  5. ^ a b c d Grønvik, S.; Hopkins, C.C.E. (1984). "Ecological investigations of the zooplankton community of Balsfjorden, northern Norway: Generation cycle, seasonal vertical distribution, and seasonal variations in body weight and carbon and nitrogen content of the copepod Metridia longa (Lubbock)". Journal of Experimental Marine Biology and Ecology. 80 (1): 93–107. doi:10.1016/0022-0981(84)90096-0.
  6. ^ a b Plourde, S; Joly, P (2008). "Comparison of in situ egg production rate in Calanus finmarchicus and Metridia longa: discriminating between methodological and species-specific effects". Marine Ecology Progress Series. 353: 165–175. doi:10.3354/meps07181.
  7. ^ a b Daase, Malin; Eiane, Ketil; Aksnes, Dag L.; Vogedes, Daniel (2008). "Vertical distribution of Calanus spp. and Metridia longa at four Arctic locations". Marine Biology Research. 4 (3): 193–207. doi:10.1080/17451000801907948. S2CID 28776833.
  8. ^ Hays, Graeme C. (1995). "Ontogenetic and seasonal variation in the diel vertical migration of the copepods Metridia lucens and Metridia longa". Limnology and Oceanography. 40 (8): 1461–1465. CiteSeerX 10.1.1.533.6615. doi:10.4319/lo.1995.40.8.1461.
  9. ^ Connelly, Tara L.; Businski, Tara N.; Deibel, Don; Parrish, Christopher C.; Trela, Piotr; Smith, Ralph (2016). "Annual cycle of lipid content and lipid class composition in zooplankton from the Beaufort Sea shelf, Canadian Arctic". Canadian Journal of Fisheries and Aquatic Sciences. 73 (5): 747–758. doi:10.1139/cjfas-2015-0333. hdl:1807/71272.
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Metridia longa: Brief Summary

provided by wikipedia EN

Metridia longa is a copepod found in the Arctic, the north Atlantic, the Pacific, and surrounding waters. The female has an average length of about 4.2 millimetres (0.17 in), and the males have an average length of about 3.5 millimetres (0.14 in).

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Distribution

provided by World Register of Marine Species
Arctic to Long Island Sound

Reference

North-West Atlantic Ocean species (NWARMS)

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Kennedy, Mary [email]

Habitat

provided by World Register of Marine Species
upper region of the mesopelagic and glacial of the Gulf and estuary

Reference

North-West Atlantic Ocean species (NWARMS)

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cc-by-4.0
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WoRMS Editorial Board
contributor
Kennedy, Mary [email]