Dytiscus latissimus and D. circumcinctus (Coleoptera,Dytiscidae) larvae as predators on three case-making caddis larvae

The predacious behaviour of Dytiscus circumcinctus and D. latissimus larvae was studied experimentally. When offered different prey simultaneously, D. latissimus larvae preferred cased caddis larvae relative to mayfly nymphs and isopods, whereas in D. circumcinctus the preference order was reversed. Notonectid nymphs and tadpoles were consumed in higher numbers by D. circumcinctus than by D. latissimus larvae. D. circumcinctus larvae and instar III larvae of D. latissimus most frequently captured caddis larvae through the case wall, whereas the instar I and II larvae of D. latissimus normally attacked the thorax of the exposed larva from above the front opening of the case. Limnephilus borealis, L. nigriceps and L. rhombicus caddis larvae differed in case structure, and they were all successfully captured by D. latissimus and D. circumcinctus instar II and III larvae. Neither capture success nor ingestion efficiency varied significantly between the two Dytiscus species or between different prey species. Instar II and III D. circumcinctus larvae had shorter reaction times than those of D. latissimus. The larger L. borealis and L. rhombicus larvae were preferred by the two last Dytiscus larval instars, and the handling time of these two prey was longer than that of L. nigriceps larvae.     

Genetic Analysis of Line x Tester Progenies Compared in Orthogonally Supplemented Efficiency Balanced Incomplete Block Designs

The theory which analyses the progenies of line X tester crossing procedure and one group of homozygous parents is presented. This analysis allows to conclude on genetics of a quantitative character of parents included in the experiment. The statistics like variance among parents, mean variance of progenies of lines, variance of tester progeny means and covariance of testers with means of their progenies can be derived. On that base one can get four different genetic parameters of variance. In a special case of experiment, it is possible to test the significance of additive variance.     

Mitochondrial phylogenetics of the goshawk Accipiter [gentilis] superspecies

The Northern Goshawk Accipiter gentilis is a medium‐sized bird of prey inhabiting boreal and temperate forests. It has a Holarctic distribution with 10 recognized subspecies. Traditionally, it has been placed within the Accipiter [gentilis] superspecies, together with Henst's Goshawk A. henstii, the Black Sparrowhawk A. melanoleucus, and Meyer's Goshawk A. meyerianus. While those four taxa are geographically separated from each other, hence referred to as allospecies, their phylogenetic relationships are still unresolved. In the present study, we performed phylogenetic analyses on the Accipiter [gentilis] superspecies, including all recognized subspecies of all four allospecies, using partial sequences of two marker loci of the mitochondrial genome, the control region and the cytochrome b gene. We found a deep split within A. gentilis into two monophyletic groups, a Nearctic clade (three subspecies) and a Palearctic clade (seven subspecies). The Palearctic clade is closely related to A. meyerianus, and together these two were more closely related to the other Old World taxa A. henstii and A. melanoleucus, which in turn were reciprocally monophyletic sister species. As a consequence, A. gentilis as usually conceived (including all Holarctic subspecies) was non‐monophyletic. We found a strong genetic homogeneity within Palearctic A. gentilis despite the fact that it comprises seven subspecies distributed from the Atlantic coast in Western Europe to Eastern Siberia. Relationships between the four clades could not be resolved unambiguously. Our results, if confirmed by more integrative data, would imply a taxonomic revision of Nearctic A. gentilis into a separate allospecies, Accipiter [gentilis] atricapillus.     

Witnessing extinction: Population genetics of the last European Rollers (Coracias garrulus) in Austria and a first phylogeographic analysis of the species across its distribution range

Due to broad‐scale habitat loss, European Rollers (Coracias garrulus) have been decreasing in numbers rapidly during the 20th century in parts of their European distribution range. In Austria, as of 2017, only a completely isolated relict population of two breeding pairs and a few non‐breeders remained in Styria compared to about 270 pairs in the 1950s. In 2018, no breeders have been recorded. Since 2002, all nestlings and adult birds in Austria have been ringed. Given the small census size, combined with lack of immigration from other populations, genetic depletion seems likely. In the present study, mitochondrial control region sequence and microsatellite data based on blood samples of nestlings from recent years were collected and compared with museum samples from historical times (when Rollers were more common and widespread in Austria) and with birds across the distribution range to arrive at a first preliminary phylogeographic dataset for the species. The mitochondrial DNA showed a decrease in variation over time in Austria, eventually reaching monomorphism, while genetic diversity of 10 microsatellite loci was higher than expected and a change in genetic structuring through time was observed. These results indicate drift effects in this relict European Roller population caused by the fast population breakdown and small population size. Our phylogeographic analysis indicates a division into a European and an Asian group, roughly (but not exactly) in accordance with the two subspecies C. garrulus garrulus (Europe) and Coracias garrulus semenowi (Asia). The lack of substructuring in the European group along with the results from nuclear DNA markers show the Austrian Rollers to be part of a formerly continuous population and opens the way to restocking the present relict population with birds from Eastern Europe (“genetic rescue”).     

Analytical approaches to determine cytochrome P450 inhibitory potential of new chemical entities in drug discovery

The use of a cassette incubation of probe substrates with human liver microsomes (HLM) - also known as the 'cocktail' approach - is becoming a widely accepted approach to determine the interaction of new chemical entities (NCEs) with cytochrome P450 enzymes (CYP450) in early drug discovery. This article describes two LC-MS/MS-based analytical methods used at the high-throughput (HT) stage and late discovery (LD) stage for analysis of 'cocktail' incubates to analyze the probe metabolites 1'-hydroxymidazolam (CYP3A4), 4'-hydroxydiclofenac (CYP2C9), dextrorphan (CYP2D6), 1'-hydroxytacrine (CYP1A2) and 4'-hydroxymephenytoin (CYP2C19). The analytical methods are advantageous over currently reported methods due to their sensitivity, shorter analyses times (<2 min/sample for the HT method and 4 min/sample for the LD method) and their ability to monitor a unique set of clinically relevant probe metabolites from a biological incubate containing low microsomal protein (0.1mg/mL). The analytical methods employ the same mobile phase, acetonitrile and 0.1% formic acid, under similar LC-MS/MS conditions. In the HT method, the chromatographic method consists of a short robust step-gradient where the probe metabolites are simultaneously and quickly eluted to enhance throughput. The probe metabolites are chromatographically resolved in the LD stage by utilizing a true linear gradient to obtain optimal peak separation. The IC50 data generated by both analytical methods using single incubations versus cocktail incubations for various test compounds are in good agreement (correlation coefficient (r2)>or=0.98). The scientist conducting the analysis is provided with a choice of method selection depending on the stage of the test compound and on whether throughput or minimizing interference from other co-eluting metabolites is the most important criterion.