We investigated variation in the Melampyrum sylvaticum group in the Carpathian and Hercynian regions using morphological and molecular tools. The aim of our study was to examine differences in the pattern of variation between the Eastern Carpathians and region of theWestern Carpathians and the Hercynian Massif. We also tested correlations between putatively taxonomically important variation in corolla colour present in the Melampyrum sylvaticum group in the Eastern Carpathian region and other morphological and molecular traits. Samples were collected from populations of the M. sylvaticum group in the Hercynian Massif and the Eastern and Western Carpathians. Morphometric analyses of the size and shape of the corolla (based on thin plate spline with sliding semilandmarks), length of the anthers and especially molecular analyses based on sequencing the nuclear ITS and trnL-trnT regions of chloroplast DNA, confirmed that the populations occurring on the opposite sides of the Eastern-Western Carpathian biogeographic boundary are very different. It is likely that the eastern and western lineages have been isolated for a long time and the extant pattern of variation with character disagreement within the border zone, originated from hybridization and introgression. The differences in corolla colour did not coincide with the variation in morphological traits or molecular markers within the North-Eastern Carpathian region. In addition, the geographical distribution of the populations with contrasting corolla colours lacked any pattern and there are populations with both corolla colours as well as plants with transitional pale-yellow flowers. Therefore, it is suggested that M. saxosum and M. herbichii, microspecies delimited on the basis of corolla colour, are conspecific. The high level of molecular variation and its pattern indicate that the M. sylvaticum group may have survived in or near the Eastern Carpathians during the Weichselian Ice Age. This hypothesis is supported by several recent phytogeographical and palaeoecological studies, which indicate the existence of a glacial refuge in the Eastern Carpathian region. Molecular uniformity of theWestern Carpathian and Hercynian populations might in contrast indicate recent (Holocene) migration from assumed perialpine refuges.
At the southern limit of its range the endangered butterfly Coenonympha oedippus inhabits grasslands (wet, dry) that differ significantly in the abundance of its larval hostplants (wet > dry) and mean annual air temperature (wet < dry). We determined the difference in the wing morphology of individuals in the two contrasting habitats to test whether and how traits associated with wing size, shape and eye like spots vary in the sexes and two ecotypes. We show that sexual dimorphism follows the same (wing size and shape, number of eyespots on forewing) or different (relative area of eyespots on hindwings) patterns in the two contrasting habitats. Irrespective of ecotype, females had larger, longer and narrower wings, and more forewing eyespots than males. Sexual dimorphism in the relative area of eyespots on hindwing was female-biased in the wet, but male-biased in the dry ecotype. Ecotype dimorphism in wing size and the relative area of eyespots on the hindwing is best explained by mean annual air temperature and abundance of host-plants. While ecotype dimorphism in wing size did not differ between sexes, neither in direction (wet > dry) or in degree, in the two sexes the relative area of eyespots on hindwing had opposite patterns (males: dry > wet; females: wet > dry) and was more pronounced in males than in females. The differences in wing shape between ecotypes were detected only in the hindwings of males, with more rounded apex in the dry than in the wet ecotype. We discuss the life-history traits, behavioural strategies and selection mechanisms, which largely account for the sex- and ecotype-specific variation in wing morphology., Jure Jugovic, Sara Zupan, Elena Bužan, Tatjana Čelik., and Obsahuje bibliografii
Preliminary results of a search for the variation of the solar granulation properties with the heliographic laitude are presented. Within errors, no changes are found in the power spectra and sizes between N-S and E-W scans.
Genetic variation for thermal plasticity plays an important role in the success or failure of a species with respect to the colonization of different thermal habitats and the ability to deal with climatic change. The aim of this paper is to study the relative contribution of the additive and non-additive components of genetic variation for the slope of the temperature reaction norm for juvenile growth rate in the springtail Orchesella cincta. We present the outcome of an artificial selection experiment for steep and flat temperature reaction norms and the results of a parent-offspring heritability experiment. There was a considerable phenotypic variation for the slope of the reaction norm. The selection experiment and the offspring to parent regression analysis, however, yielded no evidence for significant additive genetic variance. There were also no indications for maternal effects. The full-sib analysis, on the other hand, revealed a significant broad sense heritability of 0.76. An unforeseen result was that the slopes of females were steeper than those of males. This influenced the broad sense heritability of the full-sib analysis, since accidental female or male biased broods inflate the estimate of heritability. A randomization test showed that the probability level of the observed "between group" variance on the basis of the sexual differences alone was less than 10-5. From this we conclude that autosomal genetic variation played its own separate role. In conclusion, the thermal reaction norm for growth in juvenile O. cincta is not very much determined by the additive effects of a large number of independent genes, but more likely based on a still unknown but mainly non-additive, partially sex-related genetic mechanism, possibly including both dominance and epistatic effects. Hypotheses about the role of phenotypic plasticity in processes of local adaptation and speciation should thus be alert to such a complex genetic architecture.
There exists a rich literature on systems of connections and systems of vector fields, stimulated by the irimportance in geometry and physis. In the previous papers [T1], [T2] we examined a simple type of systems of vector fields, called parameter dependent vector fields, and established their varionational equation.
In this paper we generalize the above equation to the projectable system of vector fields. The material is organized as follows: in the first section the geometry of the product bundle is presented. In the second we introduce the notion of derivative along a direction and prove Theorem 1. The third section is devoted to Theorem
2, which represents the main result of the paper. Some examples are presented in the last section. In a further paper we will apply the results in order to investigate some special systems as strong systems, “nice” systems and systems of connections generated by systems of vector fields.
We study the integrability of Banach space valued strongly measurable functions defined on [0, 1]. In the case of functions f given by ∑ ∞ n=1 xnχEn , where xn are points of a Banach space and the sets En are Lebesgue measurable and pairwise disjoint subsets of [0, 1], there are well known characterizations for Bochner and Pettis integrability of f. The function f is Bochner integrable if and only if the series ∑∞ n=1 xn|En| is absolutely convergent. Unconditional convergence of the series is equivalent to Pettis integrability of f. In this paper we give some conditions for variational Henstock integrability of a certain class of such functions.
We study properties of variational measures associated with certain conditionally convergent integrals in ${\mathbb R}^m$. In particular we give a full descriptive characterization of these integrals.
Some properties of absolutely continuous variational measures associated with local systems of sets are established. The classes of functions generating such measures are described. It is shown by constructing an example that there exists a $\mathcal{P}$-adic path system that defines a differentiation basis which does not possess Ward property.