Cytokinin (CK) has been known to inhibit primary root elongation and suggested to act as an auxin antagonist in the regulation of lateral root (LR) formation. While the role of auxin in root development has been thoroughly studied, the detailed and overall description of CK effects on root system morphology, particularly that of developing lateral root primordia (LRPs), and hence its role in organogenesis is still in progress. Here we examine the effects of conditional endogenous CK overproduction on root architecture and consider its temporal aspect during the early development of Arabidopsis thaliana. We employed the pOp/LhGR system to induce ectopic ipt overexpression with a glucocorticoid dexamethasone at designated developmental points. The transient CaMV 35S>GR>ipt transactivation greatly enhanced levels of biologically active CKs of zeatin (Z)-type and identified a distinct developmental interval during which primary root elongation is susceptible to increases in endogenous CK production. Long-term CK overproduction inhibited primary root elongation by reducing quantitative parameters of primary root meristem, disturbed a characteristic graded distribution pattern of auxin response in LRPs and impaired their development. Our findings indicate the impact of perturbed endogenous CK on the regulation of asymmetric auxin distribution during LRP development and imply that there is cross-talk between auxin and CK during organogenesis in A. thaliana.

Tissue samples from 1,117 fish of 25 species were collected from 1991 through 1996 at 13 locations along the River Elbe. The principal indicator species were perch (Perca fluviatilis) (n=118), chub (Leuciscus cephalus L.) (n=113) and roach (Rutilus rutilus) (n=138). Mercury (Hg) concentrations in muscle and liver were determined by atomic absorption spectrometry. The liver/muscle index in three indicator species from heavily contaminated and lightly contaminated localities were significantly different. In fish from heavily contaminated localities, Hg was deposited preferentially in the liver (the depository for inorganic and organic forms of Hg), while in lightly contaminated areas, it was deposited preferentially in muscle.

The various oligopeptides produced by individual Microcystis clones enable the classification of individual colonies of Microcystis in distinct peptide chemotypes. The dynamics and diversity of coexisting chemotypes are regarded as major factors influencing the microcystin-content of blooms of this potentially toxic cyanobacterial genus. We compared the chemotype composition in planktonic and benthic Microcystis communities in Brno reservoir (Czech Republic) from July to November 2004 by single-colony mass spectrometry (n 5 783). Ninetytwo peptides were selected to characterize 37 chemotypes as revealed by K-means clustering. In the course of the season the Microcystis community became significantly less diverse (linear regression of Shannon indices, p , 0.001) in the pelagic, and in November two chemotypes-both of which did not contain microcystins-accounted for nearly 80% of the colonies. In contrast, other chemotypes that were dominant in the pelagic in July were no longer encountered after August, whereas some chemotypes that never accounted for high relative abundances were encountered throughout the season. The shift to some few dominant chemotypes in the pelagic was also reflected by changes in the benthic community where the same chemotypes increased in relative abundances. Nonetheless, chemotypes were identified in the sediment in July and November that were never found in plankton samples. A principal component analysis revealed that communities in the pelagial and the benthal were very different in July but converged during the season because of the deposition of dominant planktonic chemotypes in the sediment. In accordance with the declining percentage of toxin-producing Microcystis colonies, the microcystin content of seston samples decreased significantly from 0.9 mg g 21 dry weight to levels below the detection limit (linear regression, p , 0.001).

The purpose of this study was to investigate the role of wild animals for Anaplasma phagocytophilum, other ehrlichiae/anaplasmae, Rickettsia helvetica and other rickettsiae and whether different genetic variants of A. phagocytophilum in central Slovakia exist. A total of 109 spleen samples from 49 red deer (Cervus elaphus), 30 roe deer (Capreolus capreolus), 28 wild boar (Sus scrofa) and two mouflon (Ovis musimon) were collected from June 2005 to December 2006. Polymerase chain reaction (PCR) amplification of the16S rRNA gene was used for detection of ehrlichiae/anaplasmae. A nested PCR targeting part (392 bp) of groESL gene was applied for the specific detection of A. phagocytophilum. Fragments of the gltA and ompA genes (381 bp and 632 bp, respectively) were amplified to detect rickettsiae, followed by sequencing. A. phagocytophilum and R. helvetica were detected in wild animals. The prevalence of A. phagocytophilum was 50.0± 18.2% in roe deer and 53.1±14.1% in red deer. None of the 28 wild boar was PCR positive for ehrlichiae/anaplasmae. A. phagocytophilum was detected in one mouflon. R. helvetica was found in one roe deer. Our study suggests a role of cervids as a natural reservoir of A. phagocytophilum in Slovakia. However, the role of cervids and wild boars in the circulation of R. helvetica remains unknown. The analysis of sequence variation in the msp4 coding region of A. phagocytophilum showed the presence of different variants previously described in ruminants.

The species richness and composition of land snail assemblages in 42 floodplain forest sites along the Danube River in Slovakia were studied to find the main ecological gradients responsible for the variation in the faunas. We found just one, but steep, ecological gradient influencing the variation of snail species composition among different floodplain forest types, reflected in the first detrended correspondence analysis axis, which explained 29.6% of total variation. Site scores on this axis were significantly correlated with site humidity (r s ¼ 20.868; P , 0.001). Significant loading on the first axis was also found for flood frequency and several vegetation descriptors. Species composition mainly reflected differences between sites without floods and the others. Species richness as well as total abundances of live individuals were not significantly controlled by any explanatory variable, although some trends could be discerned. Considering vegetation classification, substantial differences were observed between wet softwood floodplain forests and the remaining types, drier softwood forests and different types of hardwood forests, which were impossible to distinguish based on land snail assemblages. The results are discussed in relation to earlier descriptive studies, and in terms of the conservation of these threatened habitats.