HISTORICAL FACTORS AND ANISOPLETHIC POPULATION STRUCTURE IN TRISTYLOUS PONTEDERIA CORDATA: A REASSESSMENT

Theoretical models of floral-morph frequencies in tristylous species predict a single equilibrium with all three morphs represented in equal proportions (isoplethy). North American populations of Pontederia cordata exhibit considerable heterogeneity of morph frequencies between populations, with the short-styled morph often in excess of isoplethic expectations and the long-styled morph commonly underrepresented. In a previous study, it was proposed that anisoplethic population structure in P. cordata is the result of differential male fertility, owing to genetic differences in pollen production among the morphs. In this study, the influence of historical factors on morph frequencies prior to equilibrium was investigated using a deterministic computer model. Nonequilibrium frequencies are strongly influenced by the genotypes of founding individuals, and, because tristyly is under the control of two diallelic loci, phenotypic equilibrium is approached asymptotically. The model indicates that in nonequilibrium populations the short-styled morph will be in excess and the long-styled morph will be underrepresented. This suggests that historical factors play an important role in determining population structure in P. cordata. Several features of the population ecology of the species lend support to this interpretation. Historical factors should be taken into account when interpreting data from population surveys of morph frequencies in tristylous species and of other genetic polymorphisms not under single-locus control.     

Equilibrium populations of heterostylous plants

A general relation is derived which must be satisfied by the equilibrium frequencies of the incompatibility types occurring in populations of heterostylous plants. Specific assumptions are made about the underlying genetic mechanism, but these are fulfilled in practically all relevant cases. With usual mating systems corresponding to pollen or zygote elimination and no fitness differences, it follows that all incompatibility types must be equally frequent. Given different fitness values, the general relation leads to more complex equations determining the frequencies. These equations are used for estimating fitness values of the Long, Mid and Short types in Lythrum salicaria. Expressions for the equilibrium frequencies are also found for a special mating system in Oxalis alpina.     

Conditions under Which the Mean Fertility Is Maximized When a Population Is at a Stable Equilibrium

It is assumed that there is a population with two alleles at one locus, random mating of adults and selection only involving differential fertilities. By making use of the Kuhn-Tucker theory of optimization under constraints, conditions are derived under which stable equilibrium frequencies x, y and z of the three genotypes are the same as those that maximize the mean fertility of the population. We derive all sets of frequencies of this type for the Hadeler-Liberman symmetric fertility model and all such sets for which at least one genotype is missing for the general model. If the population has frequencies that are initially near those at which there is both a stable equilibrium and maximization of the mean fertility, then the mean fertility (t) at time t is nondecreasing with t as t -> &. It is found that it is possible for the stable equilibrium maximum points (x, y, z) to be one or two points on a ridge on which the mean fertility is maximized or the entire set of points on the ridge. Furthermore, may be smaller on this ridge than at another stable equilibrium point at which is not even locally maximized.     

Density dependent selection incorporating intraspecific competition 1. A haploid model

A haploid model is introduced and analyzed in which intraspecific competition is incorporated within a density dependent framework. It is assumed that each genotype has a unique carrying capacity corresponding to the equilibrium population size when fixed for that type. Each genotypic fitness at a single multi-allelic locus is a function of a distinctive effective population size formed by adding the numbers of each genotype present, weighted by an intraspecific competition coefficient. As a result, the fitnesses depend upon the relative frequencies of the various genotypes as well as the total population size. Intergenotypic interactions can have a profound effect upon the outcome of the population. In particular, when the density effect of one individual upon another depends upon their respective genotypes, a unique stable interior equilibrium is possible in which all alleles are present. This stands in contrast to the purely density dependent haploid system in which the only possible stable state corresponds to fixation for the type with the highest carrying capacity. In the present model selective advantage is determined by a balance between carrying capacity and sensitivity to density pressures from other genotypes. Fixation for the genotype with the highest carrying capacity, for instance, will not be stable if it exerts a sufficiently weak competitive effect upon the other genotypes. In the diallelic case, maintenance of both alleles at a stable equilibrium requires that the net intragenotypic competition between individuals of like genotype be stronger than that between unlike types. As for purely density regulated systems, there may be no stable equilibria and/or regular and chaotic cycling may occur. The results may also be interpreted in terms of a discrete time model of interspecific competition with each haplotype representing a different species.     

POPULATION STRUCTURE AND MORPH-SPECIFIC FITNESS DIFFERENCES IN TRISTYLOUS LYTHRUM SALICARIA

In tristylous plant populations, style-morph frequencies are governed by an interaction between frequency-dependent selection due to disassortative mating and stochastic processes. Provided that there are no inherent fitness differences among morphs, frequency-dependent selection should result in equal morph frequencies at equilibrium. Stochastic models indicate that the short-styled morph has the highest and the long-styled morph the lowest probability of being lost from local populations as a result of random processes. We surveyed the morph composition of 82 populations of the tristylous, self-incompatible herb Lythrum salicaria in two archipelagos, one in central and one in northern Sweden, located close to the range-margin of the species. To examine whether deviations from even morph frequencies can be explained by among-morph differences in reproductive success, we quantified flower and seed production in six and three populations in the northern and southern archipelago, respectively, and we recorded segregation ratios in offspring produced in six trimorphic populations in the northern area. Seed germination and offspring growth were studied in the greenhouse. Ninety percent of the populations in the southern archipelago (N = 31) and 69% of the populations in the northern archipelago (N = 35) were trimorphic; the remaining populations were dimorphic (only populations consisting of at least three flowering plants considered). Dimorphic populations were smaller than trimorphic populations, as predicted by stochastic models. There was a striking difference in the morph composition of L. salicaria populations between the two archipelagos. In the southern archipelago, there was a slight excess of the long-styled morph and a corresponding deficiency of the short-styled morph. In contrast, the northern populations were characterized by a marked deficiency of the mid-styled morph: the average frequency of the mid-styled morph in trimorphic populations was 0.21, and nine of eleven dimorphic populations lacked the mid-styled morph. In both archipelagos, the long-styled morph (the most common morph) produced about 20% fewer seeds per fruit than the other morphs. The long-styled morph also tended to produce fewer seeds per plant. A hand-pollination experiment performed in two of the northern populations indicated that seed production per flower was pollen-limited in the long-styled morph but not in the other two morphs. Seed germination and offspring size after 24 weeks of growth did not differ among morphs. The mid-styled morph tended to have a higher representation in the offspring than in the parental generation in all six trimorphic populations studied further indicating that the deficiency of the mid-styled morph in the northern archipelago does not represent an equilibrium. Taken together, the results do not support the hypothesis that morph-specific differences in reproductive success can account for deviations from even morph frequencies in L. salicaria. It is suggested that among-morph differences in other components of fitness and historical factors may contribute to the current morph structure.     

Linkage disequilibrium and gametophytic self-incompatibility

Summary The approach to linkage equilibrium of a locus linked to the locus determining gametophytic self-incompatibility (S) is considered. For the simplest case of three alleles at the S locus and two at the linked locus it is necessary to consider 3 measures of linkage disequilibrium. These are found to approach their equilibrium value of zero in one of three ways: 1) steadily declining to zero; 2) oscillating as decline proceeds; 3) a combination: 2) followed by 1). Linkage equilibrium may be established before genotype frequencies reach their expectation under random crossing. Earlier studies (Li 1951; Moran 1962) of the approach to S allele equilibrium have been based on the assumption that all types of pollen take part in fertilizations equally frequently. Such an assumption leads to simpler expressions for changes in S gene frequencies but is extremely unrealistic and, in particular, leads to a different rate of approach to equilibrium from the more comprehensive model. It is shown that even in the absence of selection it is not possible to predict the equilibrium gene frequency of a linked locus until S allele equilibrium is reached. This frequency may be either higher or lower than that calculated from a gene count in the starting genotype pool. However, these two gene frequencies may stabilize long before linkage equilibrium is achieved. An examination of selection against one genotype at the linked locus is undertaken. If linkage is complete, lethality can be less effective at reducing the gene frequency than is less intense selection (in only a few generations of selection). Here too linkage equilibrium may be established with selection still effective in bringing about a decline in gene frequency. An examination of the analysis and conclusions of Rasmuson (1980) shows that because these were based on the inadequate formulae previously discussed and exclude phenomena discussed above, they are misleading. The possibility of a gametophytic self-incompatibility system providing a sufficient condition for the sheltering of lethals in the absence of the condition of complete linkage to the S locus (r=0) is shown to be unlikely.     

The fate of balanced,phenotypic polymorphisms in fragmented metapopulations

In large populations, genetically distinct phenotypic morphs can be maintained in equilibrium (at a 1 : 1 ratio in the simplest case) by frequency‐dependent selection, as shown by Sewall Wright. The consequences of population fragmentation on this equilibrium are not widely appreciated. Here, I use a simple computational model to emphasize that severe fragmentation biases the morph ratio towards the homozygous recessive genotype through drift in very small populations favouring the more common recessive allele. This model generalizes those developed elsewhere for heterostylous plants and major histocompatibility complex alleles, emphasizes one particular outcome and avoids the restricting assumptions of more analytical models. There are important implications for both fundamental evolutionary biology and conservation genetics. I illustrate this with a range of examples but refer particularly to shell polymorphism in snails. These examples show how habitat fragmentation could have a direct and often unappreciated effect on species at the level of their population genetics.     

Herbivory and plant community dynamics: Competitive interactions between an insect-resistant and an insect-susceptible Arabidopsis thaliana genotype

Abstract

Resistance towards herbivory is expected to influence the competitive ability and ecological success of the resistant plant, but it is unclear how this general knowledge should be incorporated into long-term ecological predictions of plant community dynamics. In order to answer such questions, the long-term ecological effects of density, competition, herbivory and their compound interactions were investigated in a model system of a transgenic herbivore-resistant Arabidopsis thaliana genotype and the isogenic herbivore-sensitive A. thaliana genotype. It was concluded that herbivory had a significant effect on the fecundity of the susceptible genotype at high plant density. The most likely long-term scenario was that the susceptible genotype outcompeted the resistant genotype. But it was also shown that herbivory could down-regulate the equilibrium density of the susceptible genotype and, when the two genotypes were coexisting, up-regulate the equilibrium density of the resistant genotype.     

FACTORS INFLUENCING FREQUENCY OF THE MID-STYLED MORPH IN TRISTYLOUS POPULATIONS OF OXALIS ALPINA

Genetic models and computer simulations suggest that modifications of incompatibility in tristylous populations of Oxalis alpina from southeastern Arizona should result in evolution of distyly, due to the inability of the mid floral morph to compete effectively with the short and long floral morphs. To evaluate this hypothesis, progeny testing of naturally pollinated individuals was carried out over a three-year period for populations with differing mid frequencies. In contrast to expectations, mids appeared in greater than expected proportions in many cases. Detailed analysis of results from two trimorphic populations where the mid form is relatively uncommon revealed that mid morphs produced far more mid progeny among their offspring than expected. Assuming that all compatible pollen has the same probability of deposition on appropriate stigmas, mid excesses were found among progeny of shorts and longs in these populations as well. In a third population where the mid form is abundant, mid excesses were not found among the progeny of mids, nor were mid excesses typical among the progeny of shorts and longs. Mid excesses among progeny of populations where the mid form is uncommon may explain retention of this form, despite incompatibility modifications that should favor evolution of distyly. Over-representation of mids may result from gametophytic selection favoring mid alleles. If this is the case, tristylous populations may be in equilibrium, with the frequencies of the three morphs determined by the balance of the opposing selective forces resulting from incompatibility modifications and gametophytic selection.     

Do group dynamics affect colour morph clines during a range shift?

Species exhibiting colour polymorphism are thought to have an ecological advantage at the landscape scale, because spatial segregation of alternatively adapted ecotypes into diverse habitats can increase the species' niche breadth and thus confer greater geographic range size. However, morph frequencies are also influenced by intrapopulational processes such as frequency‐ or density‐dependent social interactions. To identify how social feedback may affect clinal variation in morph frequencies, we investigated reciprocal interactions between morph‐specific thermal tolerance, local climatic conditions and social environments, in the context of a colour‐morph frequency cline associated with a recent range expansion in blue‐tailed damselflies (Ischnura elegans) in Sweden. Cold tolerances of gynochromes (female‐like female morph) were positively correlated with local gynochrome frequencies, suggesting a positive frequency‐dependent fitness benefit. In contrast, androchrome (male‐mimic female morph) cold tolerances were improved following recent exposure to cold weather, suggesting a beneficial environmental acclimation effect. Thus, according to an environment‐matching hypothesis for clinal variation, androchrome frequencies should therefore increase towards the (cooler) range limit. In contrast to this prediction, gynochrome frequencies increased at the expanding range limit, consistent with a positive frequency‐dependent social feedback that is beneficial when invading novel climates. Our results suggest that when phenotypes or fitnesses are affected by interactions with conspecifics, beneficial social effects on environmental tolerances may (i) facilitate range shifts, and (ii) reverse or counteract typical patterns of intraspecific interactions and environment‐matching clines observed in stable populations observed over broader geographic scales.     

Patterns of differentiation in a colour polymorphism and in neutral markers reveal rapid genetic changes in natural damselfly populations

The existence and mode of selection operating on heritable adaptive traits can be inferred by comparing population differentiation in neutral genetic variation between populations (often using F(ST) values) with the corresponding estimates for adaptive traits. Such comparisons indicate if selection acts in a diversifying way between populations, in which case differentiation in selected traits is expected to exceed differentiation in neutral markers [F(ST )(selected) > F(ST )(neutral)], or if negative frequency-dependent selection maintains genetic polymorphisms and pulls populations towards a common stable equilibrium [F(ST) (selected) < F(ST) (neutral)]. Here, we compared F(ST) values for putatively neutral data (obtained using amplified fragment length polymorphism) with estimates of differentiation in morph frequencies in the colour-polymorphic damselfly Ischnura elegans. We found that in the first year (2000), population differentiation in morph frequencies was significantly greater than differentiation in neutral loci, while in 2002 (only 2 years and 2 generations later), population differentiation in morph frequencies had decreased to a level significantly lower than differentiation in neutral loci. Genetic drift as an explanation for population differentiation in morph frequencies could thus be rejected in both years. These results indicate that the type and/or strength of selection on morph frequencies in this system can change substantially between years. We suggest that an approach to a common equilibrium morph frequency across all populations, driven by negative frequency-dependent selection, is the cause of these temporal changes. We conclude that inferences about selection obtained by comparing F(ST) values from neutral and adaptive genetic variation are most useful when spatial and temporal data are available from several populations and time points and when such information is combined with other ecological sources of data.     

Altered genotypic and phenotypic frequencies of aphid populations under enriched CO2 and O3 atmospheres

Environmental change is anticipated to negatively affect both plant and animal populations. As abiotic factors rapidly change habitat suitability, projections range from altered genetic diversity to wide-spread species loss. Here, we assess the degree to which changes in atmospheric composition associated with environmental change will influence not only the abundance, but also the genotypic/phenotypic diversity, of herbivore populations. Using free-air CO₂ and O₃ enrichment (FACE) technology, we assess numerical responses of pea aphids (Acyrthosiphon pisum) exhibiting a pink–green genetic polymorphism and an environmentally determined wing polyphenism on broad bean plants (Vicia faba) under enriched CO₂ and/or O₃ atmospheres, over multiple generations. We show that these two greenhouse gases alter not only aphid population sizes, but also genotypic and phenotypic frequencies. As the green genotype was positively influenced by elevated CO₂ levels, but the pink genotype was not, genotypic frequencies (pink morph : green morph) ranged from 1 : 1 to 9 : 1. These two genotypes also displayed marked differences in phenotypic frequencies. The pink genotype exhibited higher levels of wing induction under all atmospheric treatments, however, this polyphenism was negatively influenced by elevated O₃ levels. Resultantly, frequencies of winged phenotypes (pink morph : green morph) varied from 10 : 1 to 332 : 1. Thus, atmospheric conditions associated with environmental change may alter not just overall population sizes, but also genotypic and phenotypic frequencies of herbivore populations, thereby influencing community and ecosystem functioning.     

Female reproductive success and the evolution of mating-type frequencies in tristylous populations

In tristylous populations, mating-type frequencies are governed by negative frequency-dependent selection typically resulting in equal morph ratios at equilibrium. However, Narcissus triandrus generally exhibits long-styled (L)-biased populations with a deficiency of the mid-styled (M)-morph. Here we used a pollen-transfer model and measurements of female fertility in natural populations to investigate whether these uneven morph ratios were associated with variation in female reproductive success. Our theoretical analysis demonstrated that morph ratio bias can result from maternal fitness differences among the morphs, and that these effects were magnified by asymmetrical mating. In nine out of 15 populations of N. triandrus, seed set differed significantly among the morphs, but pollen limitation occurred in only two of 11 populations investigated. Average seed set of the M-morph was positively associated with its frequency in populations. Flower size was negatively correlated with the seed set of the M-morph. Our results suggest that interactions between mating patterns and female fertility are responsible for variation in morph frequencies and loss of the M-morph from tristylous populations of N. triandrus.     

Bisexual branching processes in a genetic context: rates of growth for Y-linked genes

A multitype bisexual branching process is considered to model the behaviour of a Y-linked gene with two genotypes in a two-sex population. It is assumed perfect fidelity mating with preference of females for the males carrying certain allele of the gene. Under these assumptions, we study the rate of growth of each genotype on the event of non-extinction. The rate of growth of a genotype may depend on whether the other survives or becomes extinct and, in general, both genotype frequencies grow at different rates. We also investigate conditions for the simultaneous explosion of both genotypes to have positive or zero probability.     

Colour polymorphism in the salt-marsh isopod,Sphaeroma rugicauda; Evidence for stable equilibrium frequencies

Summary If morph frequencies in a polymorphic population are maintained at stable equilibria, then if the frequencies are perturbed they should return to their equilibrium values. Artificial populations of the isopod were set up in cages on the salt-marsh with varying frequencies of the pattern morph. The cages were left undisturbed for five months over the breeding season. In the control cages the initial frequency of pattern (0.15) was the same as in the natural population. At the end of the experiment the frequency had not changed significantly, and was not significantly different from the frequency of pattern in the natural population (at the end of the experiment). High frequency cages started with pattern at a frequency of 0.5, showed significant decreases in frequency towards the control values, from which they were not significantly different by the end of the experiment. The average frequency in low frequency cages (started with pattern at 0.06) rose only slighly and was still significantly lower than the average control frequency by the end of the experiment. It is suggested that in these cages the restoring force may have been opposed by random processes, since pattern was lost entirely from some of the cages. The results indicate that the polymorphism is at a stable equilibrium, although the nature of the restoring forces were not identified.     

Correlated evolution of floral morphology and mating-type frequencies in a sexually polymorphic plant

In sexually polymorphic species, reproductive morphology governs mating patterns and the character of negative frequency-dependent selection. If local environmental conditions cause sexual morphs to differ between populations, then frequency-dependent selection should create corresponding geographic variation in morph frequencies. We investigate this relation with a model of morph-ratio evolution and analysis of geographic variation in the heterostylous plant Narcissus triandrus. Unlike other tristylous species, N. triandrus possesses both imperfect reciprocity among morphs in sex-organ position and a self-incompatibility system that permits outcrossing within and between morphs. We sampled 137 populations throughout the Iberian Peninsula for floral-morph ratios, and measured floral morphology in 31 populations. Morph ratios exhibited three atypical features: (1) predominance of the long-styled (L) morph; (2) absence of the mid-styled (M) morph from 17.5% of populations; and (3) a negative relation between the frequencies of the L and M morphs among populations. Morph ratios varied geographically, with decreasing frequency of the M morph from the southeast to the northwest of the species' range. Much of this variation accompanied allometric change in the positions of sex organs, especially the mid-level organs, with the M morph declining in frequency and ultimately being lost in large-flowered populations. Using multivariate multiple regression, we demonstrate that variation in floral morphology among populations predicts this geographic variation in morph frequencies. Our theoretical analysis illustrates that patterns of pollen transfer governed by imperfect sex-organ reciprocity can select for unequal equilibrium morph ratios like those observed for N. triandrus. We interpret the L-biased morph ratios and the unusual morphology of N. triandrus as a consequence of its atypical intramorph compatibility system.     

Range limits,large‐scale biogeographic variation,and localized evolutionary dynamics in a polymorphic damselfly

Studies of heritable colour polymorphisms allow investigators to track the genetic dynamics of natural populations. By comparing polymorphic populations over large geographic areas and across generations, issues about both morph stability and evolutionary dynamics can be addressed, increasing our understanding of the potential mechanisms maintaining genetic polymorphisms. In the present study, we investigated population morph frequencies in a sex‐limited heritable colour polymorphic damselfly (Ischnura elegans, Vander Linden), with three discrete female morphs. We compared the frequencies of these three female morphs in 120 different populations from ten European countries at differing latitudes and longitudes. There were pronounced differences in morph frequencies both across the entire European biogeographic range, as well as at a smaller scale within regions. We also found considerable between‐population variation at the local scale within regions, particularly at the edges of the range of this species. We discuss these findings in the context of recent models of adaptive population divergence along the range of a species. This polymorphism is thus highly dynamic, with stable morph frequencies at the core of the species range but fluctuating morph dynamics at the range limits. We finish with a discussion of how local interactions and climatic factors can be expected to have a strong influence on the biogeographic patterns in this species and other sexually selected polymorphisms. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102 , 775–785.     

Epistasis of quantitative trait loci under different gene action models

Modeling and detecting nonallelic (epistatic) effects at multiple quantitative trait loci (QTL) often assume that the study population is in zygotic equilibrium (i.e., genotypic frequencies at different loci are products of corresponding single-locus genotypic frequencies). However, zygotic associations can arise from physical linkages between different loci or from many evolutionary and demographic processes even for unlinked loci. We describe a new model that partitions the two-locus genotypic values in a zygotic disequilibrium population into equilibrium and residual portions. The residual portion is of course due to the presence of zygotic associations. The equilibrium portion has eight components including epistatic effects that can be defined under three commonly used equilibrium models, Cockerham's model, F2-metric, and F(infinity)-metric models. We evaluate our model along with these equilibrium models theoretically and empirically. While all the equilibrium models require zygotic equilibrium, Cockerham's model is the most general, allowing for Hardy-Weinberg disequilibrium and arbitrary gene frequencies at individual loci whereas F2-metric and F(infinity)-metric models require gene frequencies of one-half in a Hardy-Weinberg equilibrium population. In an F2 population with two unlinked loci, Cockerham's model is reduced to the F2-metric model and thus both have a desirable property of orthogonality among the genic effects; the genic effects under the F(infinity)-metric model are not orthogonal but they can be easily translated into those under the F2-metric model through a simple relation. Our model is reduced to these equilibrium models in the absence of zygotic associations. The results from our empirical analysis suggest that the residual genetic variance arising from zygotic associations can be substantial and may be an important source of bias in QTL mapping studies.     

Do current hypotheses explain continental and seasonal variation in female morph frequencies of the damselfly,Nehalennia irene?

Female-limited colour polymorphism occurs in many damselfly species, where one morph resembles the male (andromorph) and the other is dissimilar (gynomorph). Explanations for this phenomenon vary, but most assume that andromorphism has arisen in odonates, as a response to excessive male harassment. Here, we quantify the extent of continental and seasonal variation in female morph frequencies in a widely-distributed damselfly and ask whether the spatiotemporal patterns in andromorph frequency can be understood on the basis of sexual harassment theory. We sampled the damselfly, Nehalennia irene (Hagen) among regions across Canada, and at several sites, over the reproductive season, within Central Canada. Andromorph frequencies ranged from 0 to > 90% across Canada. In particular, sites in Western Canada had consistently high andromorph frequencies, whereas andromorph frequencies among Central sites were lower and variable and, among Eastern sites, were lower still (except one site) and relatively invariant. For populations in Central Canada, both andromorph frequencies and population densities varied significantly over time, reaching a peak mid-season. As expected, morph frequency covaried significantly with estimates of male harassment in some cases, but estimates of male harassment did not consistently account for variation in morph frequencies within all regions. Additional factors such as genetic drift may influence morph frequency at the edge of a species' range. Future work also should test, and attempt to explain causation, for seasonal variation in morph frequency.  © 2007 The Linnean Society of London, Biological Journal of the Linnean Society , 2007, 90 , 501–508.     

Survival,behaviour and spatial distribution of shell morphs in a population of the snail Brephulopsis bidens (Pulmonata)

Summary Microspatial variation of banded and unbanded shell morphs frequencies as well as number of individuals per m², mortality, migration and burrowing into the ground were examined in a population of snail Brephulopsis bidens found in South Crimea mountains (USSR). Differential values of relative survival of morphs were determined by their thermotolerance. The relative survival of the banded morph was lower at the west sites of population area (W=0.273), and increased gradually up to 1 at the east sites. Survival of the banded morph was dependent on its burrowing activity. Differences in relative survival of morphs decreased parallel with increasing general mortality of snails.Burrowing activity and intensity of migration of the banded morph were significantly higher than that in unbanded. In experiments with artificial shaded sections, the banded morph preferred shaded sections, whereas unbanded chose illuminated sites. All these differences in behaviour probably form the main factors for microspatial variation of morph frequencies.