a b s t r a c tMonitoring data on hibernating bats were aggregated for the first time across a number of European countries. These supranational trends revealed that nine out of 16 bat species examined increased at their hibernation sites in Europe between 1993 and 2011, while only one is decreasing. This is reflected in the positive trend shown by a prototype multispecies bat indicator which combined the individual species trends. Our findings suggest that after a period of strong decline in the 20th century, populations of most of the investigated bat species are stabilising or recovering, although with profound differences between European bio-geographical regions and countries. Bat populations in the Continental region have a less positive tendency, compared to those in the Atlantic region. More data from more countries may reveal whether these differences are systematical. So far, the prototype indicator covers 9 countries and 16 of the 45 bat species found in Europe. The next steps will be to refine the methodology behind the indicator and to improve the indicator's representation of European bat populations and its capacity to compare trends among biogeographic regions. This should be achieved by participation of more countries and incorporating data from additional bat species, including data collected by other surveillance methods, such as summer roost counts. Robust information on trends in bat populations at a range of geographic scales is essential to the long-term conservation of bats. Further development of this indicator will make an important contribution to conservation of bats because it will stimulate international cooperation and capacity building for monitoring and research, thus exchanging and broadening knowledge of the status of bats and improving the identification of threats.

The genetic background of long-chain n-alkane degradation was investigated in detail in strain E1, a member of the genetically unexplored Dietzia genus. A suicide vector carrying a 518-bp alkB fragment was site-specifically integrated into the E1 chromosome, and the full alkB, as well as its chromosomal environment was sequenced after plasmid rescue experiments. Four out of the nine putative genes were strongly induced by long-chain n-alkanes in wild-type E1. ORF4 encoded a natural fusion protein consisting of an integral membrane alkane hydroxylase and a rubredoxin domain. The significance of the alkB-rub gene in n-alkane degradation was investigated in phenotypic tests, and the disruption mutant strain exhibited severely impaired growth on n-C(20) alkane carbon source. The mutation was successfully complemented with the expression of intact AlkB-Rub protein, the full-length form of which was detected by simultaneous immunoblotting. The presented data furnish the first experimental evidence of the in vivo existence of an AlkB-Rub natural fusion protein, which plays a major role in long-chain n-alkane degradation.

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The complex [Cu(en) 2 (H 2 O)](sy) 2 (en)(H 2 O) 2 has been synthesized and characterized by its electronic and vibrational spectra. The molecular structure of the complex has been determined by X-ray diffraction methods. The complex crystallizes in the orthorhombic space group Pnma with unit-cell parameters a = 10.7236 (5), b = 20.4660(10), c = 14.4523(11)Å and Z = 4. In the cation, the Cu(II) ion has a distorted square pyramidal coordination with two bidendate (en) ligands forming the basal plane and a H 2 O molecule in the apical position. The complex cations and syringate anions constitute chains along the b axis in -A-B-A-fashion. The members of the chains are linked by through N-H···O hydrogen bonds. The (en) molecules are responsible for connecting adjacent layers.