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Hydrobia ulvae
Researched By
Lizzie Tyler
Data Supplied By
University of Sheffield
Refereed by
This information is not refereed.
Taxonomy
Scientific name
Hydrobia ulvae
Common name
Laver spire shell
MCS Code
W385
Recent Synonyms
Peringia ulvae
Phylum
Mollusca
Subphylum
Superclass
Class
Gastropoda
Subclass
Prosobranchia
Order
Mesogastropoda
Suborder
Family
Hydrobiidae
Genus
Hydrobia
Species
ulvae
Subspecies
Additional Information
Also known as the mud snail. Many synonyms have been used in the past but
Peringia ulvae
is the only one used recently.
Hydrobia ulvae
is now the standard usage although
Peringia
is often used as a sub-genus of
Hydrobia
.
Hydrobia neglecta
has a black 'v' mark near the tip of the tentacles.
The taxonomy of the Gastropoda has been recently revised (see Ponder & Lindberg 1997, and Taylor 1996). Ponder & Lindberg (1997) suggest that Mesogastropoda should be included in a monophyletic clade, the Caenogastropoda.
Taxonomy References
Howson & Picton, 1997
,
Graham, 1988
,
Fretter & Graham, 1994
,
Fish, 1979
,
Clay, 1960
,
Fish & Fish, 1977(a)
,
Taylor, 1996
,
Ponder & Lindberg, 1997
General Biology
Growth form
Turbinate
Feeding method
Surface deposit feeder, Sub-surface deposit feeder
Mobility/Movement
Swimmer, Crawler, Burrower, Drifter
Environmental position
Epifaunal
Typical food types
Detritus, periphytic microalgae.
Habit
Free living
Bioturbator
Not relevant
Flexibility
Low (10-45 degrees)
Fragility
Robust
Size
Very small(<1cm)
Height
Insufficient information
Growth Rate
Insufficient information
Adult dispersal potential
100-1000m
Dependency
Independent
Sociability
Gregarious
Toxic/Poisonous?
No
Additional Information
The males can be distinguished by a visible penis. Frequently found in very high densities - has been recorded up to 300,000 per square metre. Growth rate varies with time of year and with degree of parasite infestation. Parasite infestation is believed to cause increased growth rates, gigantism and altered morphology in this species. Parasitised snails may reach up to 9mm in height. Parasitism also affects behaviour, slowing locomotion and reducing burrowing activity. The feeding method of
Hydrobia ulvae
can also be classified as 'microbrowser'.
Biology References
Graham, 1988
,
Fretter & Graham, 1994
,
Clay, 1960
,
Sola, 1996
,
Huxham
et al
., 1995
,
Jensen & Mouritsen, 1992
,
Hayward & Ryland, 1990
,
Julie Bremner, unpub data
Distribution and Habitat
Distribution in Britain & Ireland
Found on all British and Irish coasts
Global distribution
Atlantic, English Channel, North Sea and Baltic. Insufficient detail available to map distribution.
Biogeographic range
Not researched
Depth range
0 - 20 m
Migratory
Non-migratory / Resident
Distribution Additional Information
Often found as high as the high level strand line in a dried blanket of green algae. They appear to be dead but rapidly revive when returned to more suitable conditions.
Hydrobia ulvae
does not undertake any true migration but considerable dispersal is possible through floating at the surface using a mucous raft. A cycle of climbing, floating and crawling up and down the shore has been hypothesised. Work by Barnes (1981) suggests however that climbing is simply part of normal browsing behaviour.
Substratum preferences
Sandy mud, Muddy sand, Mud
Physiographic preferences
Open coast, Sealoch, Ria / Voe, Estuary, Isolated saline water (Lagoon), Enclosed coast / Embayment
Biological zone
Upper Littoral Fringe, Lower Littoral Fringe, Upper Eulittoral, Mid Eulittoral, Lower Eulittoral, Sublittoral Fringe, Upper Infralittoral, Lower Infralittoral
Wave exposure
Sheltered, Very Sheltered, Extremely Sheltered, Ultra Sheltered
Tidal stream strength/Water flow
Moderately Strong (1-3 kn), Weak (<1 kn), Very Weak (negligible)
Salinity
Variable (18-40 psu), Low (<18 psu), Full (30-40 psu), Reduced (18-30 psu)
Habitat Additional Information
AMBI Group (Borja
et al.
, 2000)
III
Distribution References
Graham, 1988
,
Fretter & Graham, 1994
,
Clay, 1960
,
Barnes, 1981
,
Anderson, 1971
,
Hayward & Ryland, 1990
Reproduction/Life History
Reproductive type
Gonochoristic
Developmental mechanism
Planktotrophic, Lecithotrophic
Reproductive Season
March to October
Reproductive Location
Insufficient information
Reproductive frequency
Annual protracted
Regeneration potential
No
Life span
1-2 years
Age at reproductive maturity
<1 year
Generation time
Insufficient information
Fecundity
26.5
Egg/propagule size
Fertilization type
Internal
Larvae/Juveniles
Larval/Juvenile dispersal potential
>10km
Larval settlement period
Insufficient information
Duration of larval stage
11-30 days
Additional Information
The longevity of this species is debatable.
Hydrobia ulvae
may live up to five years in aquaria and over four years in the arctic. Various studies have suggested that it lives from just over 1 year up to 2.5 years. Individuals hatching from eggs laid in spring can breed in autumn, whereas those hatching in autumn over-winter before breeding in spring. The species is gonochoristic and sperm transfer occurs by copulation. Minimum egg hatching time has been recorded as five days. There is considerable conflicting evidence over the developmental mechanism of the larvae of this species. Some workers (Fish & Fish, 1977) have found the planktonic stage to last up to four weeks and development to be entirely planktotrophic. Others (Pilkington, 1971) have found the planktonic stage to be completely absent with a nonfeeding benthic larva that metamorphoses after just two days. Snails producing planktotrophic forms have several (7-22) smaller eggs that hatch into veliger larvae at around 150 microns. Snails producing lecithotrophic forms lay fewer (3-7) larger eggs. Maximum number of eggs recorded from one mass is 50. The timing of the breeding season varies with latitude. In the north of Scotland there is a short spawning period in Spring. In populations further south the spawning period is more protracted and is split into two peaks (spring and autumn). Age at maturity Eggs are laid preferentially on the shells of live individuals of this species but also on empty shells and grains of sand. The egg mass acquires a protective layer of sand grains.
Reproduction References
Fretter & Graham, 1994
,
Barnes, 1988
,
Clay, 1960
,
Barnes, 1990
,
Fish & Fish, 1974
,
Anderson, 1971
,
Sola, 1996
,
Pilkington, 1971
,
Eckert, 2003
,
Julie Bremner, unpub data