BIOTIC Species Information for Abra alba
Researched byLizzie Tyler Data supplied byUniversity of Sheffield
Refereed byThis information is not refereed.
Reproduction/Life History
Reproductive typeGonochoristic
Developmental mechanismPlanktotrophic
Reproductive SeasonFebruary to Autumn Reproductive LocationWater column
Reproductive frequencyAnnual protracted Regeneration potential No
Life span1-2 years Age at reproductive maturity
Generation time<1 year Fecundity17000
Egg/propagule size60 µm diameter Fertilization typeExternal
Larvae/Juveniles
Larval/Juvenile dispersal potential>10km Larval settlement periodInsufficient information
Duration of larval stage1-2 months   
Reproduction Preferences Additional InformationGametogenesis
Dewarumez (1979) and Nott (1980) described the anatomy of the gonads of Abra alba and changes in the gonad condition during the reproductive cycle.

Fertilization and metamorphosis
The sexes are separate and may be distinguished microscopically by dissection. Nott (1980) estimated the number of eggs produced from an average sized animal 11 mm in length to be between 15,000 - 17,000 of 60 µm diameter. Gametes are shed within the shell cavity and swept out through the exhalent siphon by pumping, so that fertilization occurs externally. The eggs develop into free-swimming trochophore and then veliger larvae. The larval stage is planktonic, and in Abra alba, lasts about a month (Dauvin & Gentil, 1989). Larvae are subject to very high mortality. At metamorphosis, the larvae settle out of the plankton and the bivalve spends its remaining life as a member of the benthos (Dame, 1996).

Recruitment
Recruitment varies between localities. In a population of Abra alba from the Irish Sea, proliferation of the gonads commenced in March and the animals reached maturity between June and September. The exact time at which maturity was attained depended upon the size of the individual, but it seemed that only individuals with a minimum shell length of between 7-9 mm reproduced (Nott, 1980). Normally, there two distinct spawning periods in summer and autumn, and according to the season of settlement, individuals differ in terms of growth and potential life span. Although peak recruitment usually occurs in summer (Dauvin & Gentil, 1989).
  • In Kiel Bay a recruitment peak occurred in August, sometimes with a second peak between December and February (Rainer, 1985).
  • Autumn settled individuals from the Bay of Morlaix, France, initially showed no significant growth; they were not collected on a 1 mm mesh sieve until April, 5 to 7 months after settlement. Such individuals were expected to have a maximum life span of 21 months and could produce two spawnings. In contrast, veliger larvae that settled during the summer grew very rapidly and were collected on a 1 mm mesh sieve just one month after settlement. They lived about one year and spawned only once (Dauvin & Gentil, 1989).
  • Dauvin & Gentil (1989) observed three recruitment periods (February-March, April-June and August-October) in response to trophic conditions following the Amoco Cadiz oil spill in the Bay of Morlaix, France (see sensitivity, nutrients). The additional recruitment period was considered to be an adaptive response over the normal pattern of twice yearly recruitment.
  • Two peaks (in July and September-October) were noted in the Limfjord (Jensen, 1988), with spat densities in excess of 20,000 m² recorded (see general biology).
  • Warwick & George (1980) inferred that settlement in Swansea Bay, Wales, occurred over a period of months between July and November.
Reproduction References Nott, 1980, Dauvin & Gentil, 1989, Dame, 1996, Jensen, 1988, Rees & Dare, 1993, Rainer, 1985, Warwick & George, 1980, Dewarumez, 1979,
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