Coelopa pilipes
| Coelopa pilipes | |
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Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Diptera |
| Family: | Coelopidae |
| Genus: | Coelopa |
| Species: | C. pilipes
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| Binomial name | |
| Coelopa pilipes Haliday, 1838
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Coelopa pilipes is a common European species of kelp fly first recorded by A.H. Haliday in 1838.[1] It is also known as Coelopa brevipilosa and Coelopa marina.[2] C. pilipes lives in washed-up kelp on beaches before adulthood and can recycle decaying kelp by consuming it. C. pilipes has significant sympatry with C. frigida; the two flies are often studied together due to their overlapping habitats and distribution.
Description
_plus_Kelp_Fly._Coelopa_pilipes,_Coelopidae_(39648498673).jpg)
In general, seaweed flies are dark-colored, small or medium-sized flies with hairs or bristles.[3] Darker adult color makes them more distinguishable from other species, but larvae are less easily identified.[4]: 59 They have small eyes and short antennae and legs,[3] and their bodies tend to be more flattened than that of other species. Environmental, genetic factors, and nutrition contribute to variable measurements in the fly, such as wing size.[5]: 171 In order to adapt to the seaside environments, C. pilipes larvae have hair on their posterior parts and pines on their ventral surfaces, as seen in species that dwell in damper seaweed.[6]: 455
Taxonomy
Coelopa pilipes are phylogenetically distant from other species in the Coelopa genus and thus display certain behaviors less typical of Coelopa flies.[7]
Distribution
Coelopa pilipes can be found in Eastern European countries with shorelines, such as Belgium, Britain, Denmark, France, Germany, Iceland, Ireland, Norway, and Poland. Other reported locations for C. pilipes residence include North Africa[8] and Australia, a more significant location.[5]: 176
Habitat
On beaches, C. pilipes is able to thrive within decaying seaweed, which provides a relatively warm and humid environment throughout the year. Seaweed on beaches is especially prevalent after storms and high tides in the spring.[9] Coelopa have been shown to maintain a 40 °C (104 °F) environment despite snow and ice on the beach they inhabit.[6]: 451
Home range and territoriality
Sympatry
In Britain, C. pilipes populations are always mixed with C. frigida, from adult to larval stages, in varying ratios. These numbers can depend on season, as found in northeastern populations in England.[6]: 451 Interactions with and numbers of C. pilipes in a population have been observed to affect population size of C. frigida, and vice versa. C. pilipes emergence can be greatly affected by the presence of C. frigda, including prolonged development and emergence times.[9] They are generally more numerous than C. frigda in the summer months. On average, C. pilipes takes four more days than C. frigda in order to emerge from pupation as an adult.[10]
Life history
During the summer, populations of C. pilipes decrease in number.[2] They are most abundant in the fall and winter, when seaweed is most likely to be washed on the beach. All larval instars remain in the seaweed,[6]: 451 and larval aggregations tend to not be mixed in species.[11] If the seaweed is washed back to sea, the larval population can decrease significantly. Pupation begins in drier portions of seaweed, and the development time for C. pilipes is significantly longer than that of other species such as C. frigida. Adult Coelopa flies are estimated to live around 2–4 weeks, with some variation.[6]: 452
Food resources
Larvae of C. pilipes feed on the decomposing seaweed their eggs were deposited on.[6]: 451 They may also consume bacteria found on the surface of the seaweed. If only raised on Laminaria seaweed, the flies have reduced growth due to a lower nutritious value of seaweed.[5]: 455 The Fucus seaweed that the flies prefer most is prevalent in the North Pacific.[7] The presence of Fucus can be associated with the number of C. pilipes flies at a certain site.[4]: 117
Mating
Unlike flies that mate temporally, C. pilipes is able to mate throughout the year, even during the winter, due to the constant environment of rotting seaweed on beaches. Adults are found to require both Fucus and Laminaria genera of seaweed in order to breed,[6]: 453 and seaweed induces oviposition.[7]
Male/female interaction
Fucus has been observed to increase male harassment of females in addition to duration of copulation, showing the direct influence of environment on mating. Harassment rates are directly related to mating struggles. C. pilipes males increase harassment levels with more prolonged exposure to the seaweed.[10]
Unlike other species, female C. pilipes have been shown to attempt rejection of males based on body size by performing abdominal bends. Willingness to mate can also be affected by the available varieties of seaweed.[7] Females may shake and kick to reject males; however, female resistance reduces as male harassment increases due to increased costs of resisting.[10]
Parental care
Adult C. pilipes lay their eggs after seaweed is deposited on the beach, during which initial decay creates a warmer environment on the seaweed. Larvae feed on the seaweed, promoting more decay, which attracts more females to lay their eggs.[6]: 451 Females lay eggs singly, as does Drosophila melanogaster.[11] As a result, larvae are aggregated less densely than other species. Without Fucus seaweed, females are less likely to lay eggs.[4]: 126
Enemies
Coelopa pilipes flies are prone to parasitism by the mite Thinoseius fucicola, with males being more susceptible.[12]
Genetics
Coelopa pilipes has 6 total chromosome pairs. 5 have median centromeres, and the remaining one is a dot-shaped pair. The shape of the chromosomes is relatively uniform. Heterochromatin is scattered throughout the chromosomes of C. pilipes flies, and the localization of sex-controlling genes is unknown, as there is no clear sexual dimorphism.[7]
Physiology
Exposure to certain seaweed such as Fucus has been shown to increase mortality of some kelp fly species; however, virgin C. pilipes are able to delay this effect.[citation needed]
Interactions with humans
Because C. pilipes has been successfully reared in the laboratory and contain significantly higher omega-3 polyunsaturated fatty acids, larvae have been studied for potential animal consumption as feed.[5]
References
- ^ Haliday, A. H. (1838-10-01). "XV.—New British insects indicated in Mr. Curtis's guide". Annals and Magazine of Natural History. 2 (8): 112–121. doi:10.1080/00222933809512345. ISSN 0374-5481.
- ^ a b "Catalogue of Life - 2011 Annual Checklist :: Species details". www.catalogueoflife.org. Retrieved 2019-11-01.
- ^ a b Grootaert, Patrick; De Bruyn, Luc; Meyer, Marc (1991-01-01). Catalogue of the Diptera of Belgium.
- ^ a b c Butlin, Roger Kenneth (1983). "The maintenance of an inversion polymorphism in Coelopa frigida". eprints.nottingham.ac.uk. Retrieved 2019-11-01.
- ^ a b c d Mathis, Wayne Neilsen and McAlpine, D. K. 2011. "A catalog and conspectus on the family Coelopidae (Diptera: Schizophora)." Myia. 12:171–205.
- ^ a b c d e f g h Cheng, Lanna (1976). "Marine Insects".
{{cite journal}}: Cite journal requires|journal=(help) - ^ a b c d e Dunn, Derek W.; Crean, Caroline S.; Gilburn, André s (2002). "The effects of exposure to seaweed on willingness to mate, oviposition, and longevity in seaweed flies". Ecological Entomology. 27 (5): 554–564. doi:10.1046/j.1365-2311.2002.00445.x. ISSN 1365-2311.
- ^ "Coelopa pilipes Haliday, 1838 | Fauna Europaea". fauna-eu.org. Retrieved 2019-11-01.
- ^ a b Biancarosa, I.; Liland, N.s.; Day, N.; Belghit, I.; Amlund, H.; Lock, E.-J.; Gilburn, A.s. (2018-05-29). "The chemical composition of two seaweed flies (Coelopa frigida and Coelopa pilipes) reared in the laboratory". Journal of Insects as Food and Feed. 4 (2): 135–142. doi:10.3920/JIFF2018.0008.
- ^ a b c Edward, Dominic A.; Gilburn, Andre S. (2007-08-01). "The effect of habitat composition on sexual conflict in the seaweed flies Coelopa frigida and C. pilipes". Animal Behaviour. 74 (2): 343–348. doi:10.1016/j.anbehav.2006.07.023. ISSN 0003-3472.
- ^ a b Butlin, R. K.; Collins, P. M.; Day, T. H. (1984-06-01). "The effect of larval density on an inversion polymorphism in the seaweed fly Coelopa frigida". Heredity. 52 (3): 415–423. doi:10.1038/hdy.1984.49. ISSN 1365-2540.
- ^ Gilburn, Andre S.; Stewart, Katie M.; Edward, Dominic A. (2009-12-01). "Sex-Biased Phoretic Mite Load on Two Seaweed Flies: Coelopa frigida and Coelopa pilipes". Environmental Entomology. 38 (6): 1608–1612. doi:10.1603/022.038.0612. ISSN 0046-225X.