Queen/worker thorax volume ratios were calculated in nine monogynous, seven polygynous and eight parasitic ant species in order to determine whether mode of nest founding is reflected in relative gyne size. A significant difference in this ratio was found between monogynous (independent nest founders) and polygynous and parasitic species (dependent nest founders). Thorax volume ratio in ants appears to be independent of actual gyne or worker size and can be used as a relative measure sure of colony investment in the gynes. Furthermore, thorax volume ratio seems to reflect the mode of nestfounding behaviour when compared between species within genera as well as among species in general. Polygyny is discussed as a nest-founding strategy that is selected for when nest founding by single gynes is difficult and costly. In addition, secondary benefits could be gained by polygynous colonies since investment in gyne size could be decreased.

Summary27 nests of Leptothorax acervorum were analysed for restriction fragment-length polymorphism (RFLP) in mitochondrial DNA (mtDNA), using four endonucleases. A substantial degree of variation was found between nests in the population (13 composite haplotypes). Intra-nest variation was detected in 15 % of the nests. The presence of occasional alien inseminated females indicates that polygyny in this species is caused by adoption of mated females. The occasional acceptance of alien females is difficult to explain, but interesting, since this behaviour could have given rise to inquilinism. Our results suggest that analysis of mtDNA RFLP is a method well suited for investigations of the population structure of ants.

Analysis of restriction fragment length polymorphism (RFLP) in mitochondrial DNA (mtDNA) in a population of Leptothorax acervorum demonstrates substantial population substructuring. Digestion with four restriction endonucleases, HaeIII, MboI, MspI and RsaI, gave six, four, three and two different patterns, respectively. Seven composite haplotypes were obtained from the observed cleavage patterns. Uniform aggregations of nests from the same maternal lineage (i.e. with the same haplotype) were found which suggests that nest-founding by a process of budding-off is common. Groups of nests seem to actively exclude other haplotypes from establishing nests within their territory. F-statistics suggests that individuals mate at random within the population.

There is high within-nest relatedness for functional queens (with corpora lutea), nonfunctional queens (without corpora lutea), and workers in polygynous nests of Leptothorax acervorum. The high functional queen relatedness suggests that young mated queens are adopted back to their mother nest. Functional queen relatedness does not change with the number of queens present in the nest, suggesting that the number of generations of queens, on average two to three, is rather stable. Worker relatedness decreases with increasing number of functional queens per nest (Tables 5, 6). The number of queens contributing offspring to the nest (mothers), estimated from worker and functional queen relatedness, is lower than the number of functional queens, particularly in highly polygynous nests. Estimates of number of mothers in monogynous nests indicate that these nests previously were polygynous (Table 7). There is no correlation between nest relatedness and distance between nests, and budding-off, if present, thus appears to be a rare mode of nest founding (Table 8). There are no indications of inbreeding in the two populations studied since the frequency of heterozygotes is as high as expected from random mating (Table 4). Most likely, polygyny is the rule in L. acervorum and serves to secure the presence of queens in the nest.

We analysed the effects of body mass on the monthly activity patterns of six Mediterranean lacertid lizard taxa, four relatively small species, the Italian wall lizard (Podarcis siculus), the common wall lizard (Podarcis muralis), the blue-throated keeled lizard (Algyroides nigropunctatus), and the Ionian wall lizard (Podarcis ionicus), and two larger species, the western green lizard (Lacerta bilineata) and the Balkan green lizard (Lacerta trilineata). The highest number of observations for all six species occurred in April and May and the lowest in July and August, the latter being the hottest and driest months of the year. The two larger species were mainly active from March to July, whereas the four smaller species had an additional period of high activity from September to November. As all six species reproduce during spring, the increase in activity of the smaller species in autumn was consequently unrelated to reproductive behaviour. There was no difference in seasonal activity of the two smaller Italian species at sites with or without the larger green lizards. It is therefore unlikely that interference competition/predation by green lizards caused the increased autumnal activity of the smaller lizards. We suggest that due to their lower mass-specific metabolic rates, larger species can obtain sufficient lipid stores over a shorter annual activity to ensure successful reproduction the subsequent spring. By contrast, smaller species have greater need to replenish their lipid reserves after summer fasting and therefore resume much higher activity levels in September to November to attain this goal.