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Echinus esculentus
Researched By
Dr Harvey Tyler-Walters and Lizzie Tyler
Data Supplied By
MarLIN and University of Sheffield
Refereed by
This information is not refereed.
Taxonomy
Scientific name
Echinus esculentus
Common name
Edible sea urchin
MCS Code
ZB198
Recent Synonyms
None
Phylum
Echinodermata
Subphylum
Echinozoa
Superclass
Class
Echinoidea
Subclass
Order
Echinoida
Suborder
Family
Echinidae
Genus
Echinus
Species
esculentus
Subspecies
Additional Information
The genus
Echinus
is derived from the Greek 'echinos' meaning 'a hedgehog'. An omnivorous grazer feeding on seaweeds (e.g.
Laminaria
spp. sporelings), Bryozoa, barnacles and other encrusting invertebrates. Size range varies depending on age and locality, e.g. c. 4 cm at 1 year, 4-7 cm at 2 years, 7 -9 cm at 3 years and 9-11 cm at 4 years. This species may hybridize with
Echinus acutus
if sympatric.
Taxonomy References
Hayward & Ryland, 1995b
,
Howson & Picton, 1997
,
Mortensen, 1927
,
Fish & Fish, 1996
,
Hyman, 1955
,
Nichols, 1969
General Biology
Growth form
Globose
Feeding method
Grazer (grains/particles), Grazer (fronds/blades), Grazer (surface/substratum)
Mobility/Movement
Crawler
Environmental position
Epifaunal
Typical food types
Recorded feeding on; worms, barnacles (e.g.
Balanus
spp.), hydroids, tunicates, bryozoans (e.g.
Membranipora
spp.), macroalgae (e.g.
Laminaria
spp.), bottom material and detritus (reviewed by Lawrence 1975).
Habit
Free living
Bioturbator
Not relevant
Flexibility
None (< 10 degrees)
Fragility
Fragile
Size
Medium(11-20 cm)
Height
Growth Rate
See additional information
Adult dispersal potential
1km-10km
Dependency
Independent
Sociability
Gregarious
Toxic/Poisonous?
No
Additional Information
Growth rates are variable depending on time of larval settlement, food availability, water temperature and age. Growth rates vary with locality although there is evidence to suggest that largest specimens are found in the south west (Nichols 1979). Growth rates based on growth lines in skeletal plates are probably underestimates (Gage 1992a & b). In the UK population growth is continuous in the first year after metamorphosis and considerably faster than adults in their 2nd year. In adults maximal growth occurs in a few months in spring and early summer but mature adults are slow growing. Comely & Ansell (1988) recorded 28 invertebrate species associated with
Echinus esculentus
from the west cost of Scotland near Oban. These included the parasites
Echinomermella grayi
and
Euonyx chelatus
mentioned above and in additional; 4 species of commensal polychaetes, a copepod and 10 amphipod species. The polychaete
Adyte assimilis
and the copepod
Pseudoanthessius liber
were regular commensals amongst the spines. Hyman (1955) states that
Echinus esculentus
is often infested with parasitic copepods e.g.
Asterocheres echinola
.
Biology References
Hayward & Ryland, 1995b
,
Mortensen, 1927
,
Fish & Fish, 1996
,
Lawrence, 1975
,
MacBride, 1903
,
Kozloff & Westervelt, 1990
,
Comely & Ansell, 1988
,
Hyman, 1955
,
Gage, 1992(a)
,
Gage, 1992(b)
,
Nichols, 1979
,
Nichols, 1969
,
Emson & Moore, 1998
,
MacBride, 1914
,
Nichols, 1984
,
Boolootian, 1966
,
Birkett
et al
., 1998b
,
Hayward & Ryland, 1990
,
Julie Bremner, unpub data
,
Mortensen, 1927
,
Rees & Dare, 1993
Distribution and Habitat
Distribution in Britain & Ireland
Common on most coasts of the British Isles but absent from most of east coast of England, the eastern English Channel and some parts of north Wales.
Global distribution
Abundant in the N.E. Atlantic from Iceland, north to Finmark, Norway and south to Portugal. Absent from the Mediterranean.
Biogeographic range
Not researched
Depth range
0 - 1200 m
Migratory
Non-migratory / Resident
Distribution Additional Information
No text entered
Substratum preferences
Bedrock, Large to very large boulders, Small boulders, Artificial (e.g. metal/wood/concrete), Rockpools, Under boulders, Caves, Crevices / fissures, Overhangs
Physiographic preferences
Open coast, Strait / sound, Sealoch, Ria / Voe, Enclosed coast / Embayment
Biological zone
Sublittoral Fringe, Upper Infralittoral, Lower Infralittoral, Upper Circalittoral, Lower Circalittoral
Wave exposure
Exposed, Moderately Exposed, Sheltered
Tidal stream strength/Water flow
Moderately Strong (1-3 kn)
Salinity
Full (30-40 psu)
Habitat Additional Information
AMBI Group (Borja
et al.
, 2000)
I
Distribution References
Hayward & Ryland, 1995b
,
Mortensen, 1927
,
Fish & Fish, 1996
,
Hyman, 1955
,
Nichols, 1979
,
Nichols, 1969
,
Nichols, 1984
,
JNCC, 1999
,
Picton & Costello, 1998
,
NBN, 2002
,
Hayward & Ryland, 1990
,
Julie Bremner, unpub data
Reproduction/Life History
Reproductive type
Gonochoristic
Developmental mechanism
Planktotrophic
Reproductive Season
Spring
Reproductive Location
Water column
Reproductive frequency
Annual episodic
Regeneration potential
No
Life span
6-10 years
Age at reproductive maturity
1-2 years
Generation time
1-2 years
Fecundity
20000000
Egg/propagule size
Fertilization type
External
Larvae/Juveniles
Larval/Juvenile dispersal potential
>10km
Larval settlement period
Duration of larval stage
1-2 months
Additional Information
Nichols (1979) estimates the maximum life span to be between 8-10 years, whereas Gage (1992a) reports a specimen (based on growth bands) of at least 16 years of age.
The number of eggs produced will vary with location and nutritive state of the adult but it is likely to be high. MacBride (1903) states that a well-grown female contains about 20 million eggs.
Maximum spawning occurs in spring although individuals may spawn over a protracted period. Gonad weight is maximal in February / March in English Channel (Comely & Ansell 1989) but decreases during spawning in spring and then increases again through summer and winter until the next spawning; there is no resting phase. Spawning occurs just before the seasonal rise in temperature in temperate zones but is probably not triggered by rising temperature (Bishop 1985). Spawning may coincide with spring phytoplankton bloom although there is no evidence to substantiate this suggestion.
Comely & Ansell (1989) demonstrated differences in reproductive condition between sites and habitats. Emson & Moore (1998) noted that gonad size varied with diet in the Isle of Cumbrae, Scotland; specimens feeding on barnacles had a higher gonad index than those feeding within the kelp forest.
Planktonic development is complex and takes between 45 -60 days in captivity (MacBride 1914). Development includes a blastula, gastrula and a characteristic, four armed echinopluteus stage that forms an important component of the zooplankton. The development of
Echinus esculentus
is described in detail by MacBride (1903, 1914). Photographs of the echinopluteus and fully formed juveniles are given by Todd
et al.
(1996).
Recruitment is sporadic or variable depending on locality, e.g. Millport populations showed annual recruitment, whereas few recruits were found in Plymouth populations during Nichols studies between 1980-1981 (Nichols 1984). Bishop & Earll (1984) suggested that the population of
Echinus esculentus
at St Abbs had a high density and recruited regularly whereas the Skomer population was sparse, ageing and had probably not successfully recruited larvae in the previous 6 years.
Settlement is thought to occur in autumn and winter (Comely & Ansell, 1988). Newly settled juveniles have an ambital diameter of 0.68 - 0.95mm (Nichols 1984).
Comely & Ansell (1988) noted that the largest number of
Echinus esculentus
occurred below the kelp forest. Similarly, Lang & Mann (1978) noted that young
Strongylocentrotus droebachiensis
recruited in urchin barrens, suggesting that urchin recruitment is improved in the absence of kelp, presumably due to differences in microclimate, the absence of suspension feeders and other predators associated with kelp beds.
Reproduction References
Lawrence, 1975
,
MacBride, 1903
,
Hyman, 1955
,
Gage, 1992(a)
,
Gage, 1992(b)
,
Nichols, 1979
,
Nichols, 1969
,
Emson & Moore, 1998
,
MacBride, 1914
,
Nichols, 1984
,
Lang & Mann, 1978
,
Bishop, 1985
,
Boolootian, 1966
,
Bishop & Earll, 1984
,
Todd
et al
., 1996
,
Julie Bremner, unpub data
,
Rees & Dare, 1993