The fragmentation of landscapes has an important impact on the conservation of biodiversity, and the genetic diversity is an important factor for a populations viability, influenced by the landscape structure. However, different species with differing ecological demands react rather different on the same landscape pattern. To address this feature, we studied three skipper species with differing habitat requirements (Lulworth Skipper Thymelicus acteon: a habitat specialist with low dispersal ability, Small Skipper Thymelicus sylvestris: a habitat generalist with low dispersal ability, Essex Skipper Thymelicus lineola: a habitat generalist with higher dispersal ability). We analysed 18 allozyme loci for 1,063 individuals in our western German study region with adjoining areas in Luxembourg and north-eastern France. The genetic diversity of all three species were intermediate in comparison with other butterfly species. The F ST was relatively high for T. acteon (5.1%), low for T. sylvestris (1.6%) and not significant for T. lineola. Isolation by distance analyses revealed a significant correlation for T. sylvestris explaining 20.3% of its differentiation, but no such structure was found for the two other species. Most likely, the high dispersal ability of T. lineola in comparison with T. sylvestris leads to a more or less panmictic structure and hence impedes isolation by distance. On the other hand, the isolation of the populations of T. acteon seems to be so strict that the populations develop independently. Although no general genetic impoverishing was observed for the endangered T. acteon, small populations had significantly lower genetic diversities than big populations, and therefore the high degree of isolation among populations might threaten its local and regional survival.

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Mountain species have evolved important genetic differentiation due to past climatic fluctuations. The genetic uniqueness of many of these lineages is now at risk due to global warming. Here, we analyse allozyme polymorphisms of 1306 individuals (36 populations) of the mountain butterfly Erebia manto and perform Species Distribution Models (SDMs). As a consensus of analyses, we obtained six most likely genetic clusters: (i) Pyrenees with Massif Central; (ii) Vosges; (iii-v) Alps including the Slovakian Carpathians; (vi) southern Carpathians. The Vosges population showed the strongest genetic split from all other populations, being almost as strong as the split between E. manto and its sister species Erebia eriphyle. The distinctiveness of the Pyrenees-Massif Central group and of the southern Carpathians group from all other groups is also quite high. All three groups are assumed to have survived more than one full glacial-interglacial cycle close to their current distributions with up-hill and down-slope shifts conforming climatic conditions. In contrast with these well-differentiated groups, the three groups present in the Alps and the Slovakian Carpathians show a much shallower genetic structure and thus also should be of a more recent origin. As predicted by our SDM projections, rising temperatures will strongly impact the distribution of E. manto. While the populations in the Alps are predicted to shrink, the survival of the three lineages present here should not be at risk. The situation of the three other lineages is quite different. All models predict the extinction of the Vosges lineage in the wake of global warming, and also the southern Carpathians and Pyrenees-Massif Central lineages might be at high risk to disappear. Thus, albeit global warming will therefore be unlikely to threaten E. manto as a species, an important proportion of the species' intraspecific differentiation and thus uniqueness might be lost.

Multi-locus monomorphism in microsatellites is practically non-existent, with one notable exception, the island fox (Urocyon littoralis dickeyi) population on San Nicolas island off the coast of southern California, having been called ''the most monomorphic sexually reproducing animal population yet reported''. Here, we present the unprecedented long-term monomorphism in relict populations of the highly endangered Parnassius apollo butterfly, which is protected by CITES and classified as ''threatened'' by the IUCN. The species is disjunctly distributed throughout the western Palaearctic and has occurred in several small remnant populations outside its main distribution area. We screened 78 individuals from 1 such relict area (Mosel valley, Germany) at 16 allozyme and 6 microsatellite loci with the latter known to be polymorphic in this species elsewhere. From the same area, we also genotyped 55 museum specimens sampled from 1895 to 1989 to compare historical and present levels of genetic diversity. However, none of all these temporal populations yielded any polymorphism. Thus, present and historical butterflies were completely monomorphic for the same fixed allele. This is the second study to report multi-locus monomorphism for microsatellites in an animal population and the first one to prove this monomorphism not to be the consequence of recent factors. Possible explanations for our results are a very low long-term effective population size and/or a strong historic bottleneck or founder event.Since the studied population has just recovered from a recent population breakdown (second half of twentieth century) and no signs of inbreeding depression have been detected, natural selection might have purged the population of weakly deleterious alleles, thus rendering it less susceptible to the usual negative corollaries of high levels of homozygosity and low effective population size.

Many studies on the biogeography of thermophilic and arctic-alpine species were performed during the past. Only little is known about species with intermediate characteristics. We analyzed the molecular biogeography of the butterfly Erebia alberganus (30 populations, representing 1106 individuals), sampled over the Alps, Apennines (Italy), and the Stara Planina (Bulgaria) using allozyme electrophoresis (17 loci). Genetic analyses revealed 3 major splits, with the strongest between the Stara Planina populations and all other populations, and a weaker split between the Alps and the Apennines. Individuals from the Apennines were genetically nested within the Alps group. The Alps cluster was segregated into 3 groups: the Southwestern, Western/Central, and Eastern Alps. The genetic diversities were highest for the Alps populations and significantly lower in the 2 isolates (Apennines, Stara Planina). The remarkable genetic split between Stara Planina and all other populations and the genetic distinctiveness of the former cluster might be interpreted as an ancient colonization event of this Balkan mountain range. The Apennines populations derive from a more recent expansion out of the Southwestern Alps. After surviving the Würm ice age most probably in the central Apennines, accompanied by genetic modification of some of these populations, northward expansion might have started from the western parts of the central Apennines reaching the northern Apennines during the early postglacial. The subtle genetic differentiation found among the Alps populations probably reflects 3 geographically disjunct Würm glacial centers located at the western slopes of the Southwestern Alps, at the southern slopes of the Central Alps, and in the Southeastern Alps.

Quaternary climatic oscillations caused severe range expansions and retractions of European biota. During the cold phases, most species shifted to lower latitudes and altitudes, and expanded their distribution range northwards and to higher elevations during the warmer interglacial phases. These range shifts produced contrasting distribution dynamics, forming geographically restricted distribution patterns but also panmictic distributions, strongly dependent on the ecologic demands of the species. The two closely related butterfly species Erebia ottomana Herrich-Schäffer, 1847 and Erebia cassioides (Reiner & Hohenwarth, 1792) show subalpine and alpine distribution settings, respectively. Erebia ottomana is found up to the treeline (1400-2400 m a.s.l.), whereas E. cassioides reaches much higher elevations (from about 1800 m a.s.l. in the Retezat Mountains, in Romania, to 2800 m a.s.l.). Thus, both species cover diverging climatic niches, and thus might also have been distributed differently during the cold glacial stages. Individuals of these two species were sampled over the mountain areas of the Balkan Peninsula and genetically analysed using allozyme electrophoresis. Additionally, we performed species distribution models (SDMs) to simulate the distribution patterns of both species in the past (i.e. during the Last Glacial Maximum and the Atlanticum). Our genetic data show contrasting structures, with comparatively low genetic differentiation but high genetic diversity found in E. ottomana, and with stronger genetic differentiation and a lower level of genetic diversity, including many endemic alleles, occurring restricted to single mountain massifs in E. cassioides. The SDMs support a downhill shift during glacial periods, especially for E. ottomana, with possible interconnection among mountain regions. We conclude that during the cold glacial phases, both species are assumed to shift downhill, but persisted at different elevations, with E. ottomana reaching the foothills and spreading over major parts of the Balkan Peninsula. In contrast, E. cassioides (the truly alpine species) survived in the foothills, but did not reach and spread over lowland areas. This more widespread distribution at the Balkan Peninsula of E. ottomana compared with E. cassioides is strongly supported by our distribution models. As a consequence, long-term geographic restriction to distinct mountain massifs in E. cassioides versus panmixia in E. ottomana produced two contrasting evolutionary scenarios.

Glacial and interglacial cycles of the Pleistocene have led to severe range fluctuations of many species. These range shifts of the past often are reflected by extant genetic signatures. Retractions of distribution areas often have fostered splits into several small and isolated retreats as remnants of the formerly interconnected range. These processes often go in line with losses of intraspecific diversity. By contrast, large and interconnected distribution ranges mostly sustain high levels of genetic variability. The genetic impact of both scenarios strongly depends on the temporal scale. In the present study, we tested the genetic effects of an assumed long-lasting widespread distribution during glacial periods and more short-term population retractions to mountain archipelagos during warm stages. We analyzed polymorphic allozymes for individuals of the Eastern Large Heath butterfly, Coenonympha rhodopensis, including major parts of its distribution, such as central Italy and the Balkan Peninsula. Our data show extraordinarily high genetic diversity. The only remarkable genetic split is detectable between the central Apennines (Italy) and the Balkan mountain systems. The populations sampled over seven Balkan mountain systems (Jakupica, Shar Planina, Ossogovo, Pirin, Rila, Rhodopes, and Stara Planina) show low genetic differentiation. This low genetic differentiation and high genetic diversity diverges from the genetic structures frequently found in species with disjunct distributions. We therefore hypothesize that the obtained molecular structure is the product of down-slope shift during the last cold stage and subsequent expansion over the lowlands of the Balkan Peninsula. The current mountain restriction most probably occurred with the beginning of the postglacial warming, which is too short a time span to be of evolutionary relevance. Therefore, the recent high genetic diversities and low differentiation may still reflect long-lasting glacial panmixia but not (yet) the recent disjunction. The strong genetic differentiation between the Balkans and Italian Apennines must result from an earlier dispersal process, most probably from the Balkans to Italy.