Hyale prevostii

Researched ByJacqueline HillData Supplied ByMarLIN
Refereed byProf. P. Geoff Moore
Taxonomy
Scientific nameHyale prevostiiCommon nameAn amphipod
MCS CodeS224Recent SynonymsHyale nilssoni (Rathke)
PhylumCrustaceaSubphylum
SuperclassClassEumalacostraca
SubclassPeracaridaOrderAmphipoda
SuborderGammarideaFamilyHyalidae
GenusHyaleSpeciesprevostii
Subspecies  
Additional InformationNo text entered
Taxonomy References Howson & Picton, 1997, Lincoln, 1979, Hayward & Ryland, 1995b
General Biology
Growth formArticulateFeeding methodHerbivore
Mobility/MovementCrawler, SwimmerEnvironmental positionEpifaunal, Epifloral, Epibenthic
Typical food typesMacroalgae, typically fucoids such as Pelvetia canaliculata and Fucus spiralis. Juveniles graze filamentous algae and micro-epiflora.HabitFree living
BioturbatorNot relevantFlexibilityHigh (>45 degrees)
FragilityIntermediateSizeVery small(<1cm)
HeightInsufficient informationGrowth RateInsufficient information
Adult dispersal potential100-1000mDependencyIndependent
SociabilityGregarious
Toxic/Poisonous?No
Additional InformationGrowth rate is affected by temperature. At higher temperatures growth is rapid with a short life span and smaller final body size (Moore, 1986).
Biology References Moore, 1986, Moore, 1977(b)
Distribution and Habitat
Distribution in Britain & IrelandAll coasts of Britain and Ireland.
Global distributionIn Europe from southwest Iceland, north Norway and the Faeroes to the Mediterranean Sea. On the Atlantic coast of north America from south Labrador and the St Lawrence estuary to Connecticut. May be locally common.
Biogeographic rangeNot researchedDepth rangeNot relevant
MigratorySeasonal (environment)
Distribution Additional InformationHyale prevostii nestles in the damp apertures of live gastropods particularly during neap tides, vacating them at spring tide when the species migrates to higher levels of the shore (Moore, 1977).
Substratum preferencesOther species (see additional information), Algae, BedrockPhysiographic preferencesOpen coast, Estuary, Strait / sound, Enclosed coast / Embayment
Biological zoneUpper Eulittoral, Mid Eulittoral, Lower EulittoralWave exposureModerately Exposed, Sheltered, Very Sheltered, Extremely Sheltered
Tidal stream strength/Water flowStrong (3-6 kn), Moderately Strong (1-3 kn), Weak (<1 kn), Very Weak (negligible)SalinityReduced (18-30 psu), Variable (18-40 psu), Full (30-40 psu)
Habitat Additional Information
Distribution References Lincoln, 1979, Hayward & Ryland, 1995b, Eno et al., 1997, Moore, 1986, Moore, 1977(c)
Reproduction/Life History
Reproductive typeGonochoristic Developmental mechanismDirect Development
Reproductive SeasonSee additional informationReproductive LocationAs adult
Reproductive frequencyAnnual protracted Regeneration potentialNo
Life span1-2 yearsAge at reproductive maturityInsufficient information
Generation time1-2 yearsFecundityInsufficient information
Egg/propagule sizeInsufficient informationFertilization typeExternal
Larvae/Juveniles
Larval/Juvenile dispersal potentialInsufficient informationLarval settlement periodNot relevant
Duration of larval stageNot relevant  
Additional Information
  • Timing and length of the reproductive period is influenced by temperature. In the south of its range, on the north coast of Spain, Hyale prevostii breeds year-round (Gonzáles & Anadón, 1981). In cooler waters the reproductive period is reduced, for example, February-November in Scotland (Moore, 1986) and April - October in New England (McBane & Crocker, 1984).
  • Reproduction, and therefore the production of gametes, varies across its range.
  • The mating system is polygynous. Mating is prefaced by a period of precopula (duration c.42h) during which time the male carries the passive female tucked under the ventral surface (Moore, 1986).
  • There is no sperm storage, and fertilisation is external.
  • Amphipods do not have a free swimming larval stage. Embryos are brooded in a marsupium, beneath the thorax, formed by the coxal plates and released as juveniles.
  • Same size females produce fewer eggs both to the far north and far south of their range supporting the hypothesis that optimal conditions exist in the middle of the species' geographical range.
Reproduction References Fish & Fish, 1996, Moore, 1986, Gonzáles & Anadón, 1981, McBane & Crocker, 1984