GEOGRAPHICAL PATTERNS OF GENETIC DIFFERENTIATION IN THE LANDSNAIL HELIX ASPERSA MuLLER (GASTROPODA: PULMONATA)

In order to investigate the initial processes responsible forthe geographical distribution of the Mediterranean landsnailHelix aspersa, populations from 64 locations in Maghreb andin Europe were studied at 17 enzyme loci by both starch andpolyacrylamide gel electrophoresis. Allele frequencies and genotypedistributions were analysed to provide information on populationstructure and genetic differentiation among populations. Valuesof Nei's unbiased (D) and Rogers (R) genetic distances led tothe formation of two main groups, namely Europe-west Algeriaand east Maghreb (average D = 0.182). Such splitting supportedthe pattern of anatomical variation recently described. Twosamples from Morocco were excluded from these groups becauseof an average D = 0.224. Within this Moroccan entity, geneticdivergences did not distinguish the ‘giant’ snailsH. a.maxima from the brownsnails H. a. aspersa. Such biochemicalsimilarities among morphological heterogeneity throws the subspecificstatus of H. a. maxima into question. Values of fixation indicesindicated that the greatest differentiation between samplesoccurred on the Maghreb territory ( = 0.393). The patterns of population differentiation are discussed inrelation to past geological and historical events. Thus, threescenarios, not mutually exclusive, are considered: the disjunctionof populations by plate tectonics during the Tertiary, the formationof geographically isolated populations during the Pleistoceneglacial/interglacial cycle and the possibility of human introductionas early as the Neolithic period. (Received 9 December 1992; accepted 11 November 1993)     

ALLOZYME VARIATION IN SOME POPULATIONS OF THE FRESHWATER SNAILS LYMNAEA PEREGRA, L. AURICULARIA AND L. STAGNALIS (GASTROPODA: PULMONATA)

Three species of the genus Lymnaea (Gastropoda, Pulmonata, Basommatophora)were examined for genetic variation at 11 enzymatic loci insamples collected in Brittany (North-Western France). Variabilitywas greatest in L. percgra, but the limited area of samplingdid not allow specific inferences. The UPGMA clustering of unbiasedgenetic distances (Nei, 1978) isolated first L. auriculariasamples, and secondly the single L. stagnalis sample from theL. peregra set. This scheme of relationships was opposed tothe identification of alleles shared by the three species atthe studied loci Analysis of L. peregra population structure by F-statistics(Weir & Cockerham, 1984) suggested high inbreeding and raisedthe possible role of self-fertilization. The contradiction betweenhigh variability and high homozygosity is discussed. Furthermore,population differentiation was rather weak (although statisticallysignificant), despite some remarkable differences among loci.Nm estimates using Wright's (1951) and Slatkin's (1985) methodsrevealed a gene flow unable to prevent the effect of geneticdrift among populations. The relative homogeneity of populationswith weak genetic exchange is discussed (Received 24 May 1993; accepted 21 March 1994)