Tissue specific variation of C-glycosylflavone patterns in oat leaves as influenced by the environment

A comparison is made between the flavone patterns accumulating in epidermal tissues and in the mesophyll of oat primary leaves grown in a phytotron and under field conditions. In developing leaves cultivated under standard conditions, varying patterns of two vitexin-derived O-rhamnosides and of one isovitexin O-arabinoside are produced in the basal region as the result of basal meristem activity. These patterns are tissue specific and differ quantitatively in the epidermis and the mesophyll. During the course of subsequent growth and differentiation, this pattern is constant as the compounds are moved upwards due to basipetal leaf growth. In comparison, the flavone patterns generated in the basal section of leaves grown in the field do not vary significantly. There is the additional accumulation of isoorientin O-arabinoside. Again flavone patterns are tissue specific, but in contrast to standard growth they are modified characteristically in those leaf tissues which are already morphologically differentiated. It is possible that the isovitexin moiety of the O-arabinoside is oxidized to the corresponding isoorientin derivative in the mesophyll. Moreover, field-grown leaves show a two-fold increase in flavone content in each leaf epidermis and a six-fold increase in the mesophyll when compared to the corresponding tissues of phytotron-grown leaves.     

Specific inhibition of outgrowth of Bacillus subtilis spores by novobiocin.

Spores of a Bacillus subtilis mutant temperature sensitive in deoxyribonucleic acid (DNA) replication proceeded through outgrowth at the nonpermissive temperature to the same extent as the wild-type parent spores. In contrast, the DNA synthesis inhibitor novobiocin completely prevented spore outgrowth while displaying a marginal effect on logarithmic growth during one generation time. Inhibition of outgrowth by novobiocin occurred in the absence of DNA replication, as demonstrated in an experiment with spores of the temperature-sensitive DNA synthesis mutant at the restrictive temperature. Novobiocin inhibited the initial rate of ribonucleic acid synthesis to the same extent in germinated spores and in exponentially growing cells. A novobiocin-resistant mutant underwent normal outgrowth in the presence of novobiocin. Therefore, novobiocin inhibition was independent of its effect on chromosome replication per se.     

Der Zug des Sperbers(Accipiter nisus) auf Helgoland

Zusammenfassung Der Sperber ist auf Helgoland nur Durchzügler. Im langjährigen Mittel werden pro Jahr im Winter 0,4, auf dem Heimzug 2,1 und im Herbst 23,0 Fänglinge festgestellt. Der Zugablauf läßt eine Trennung der Zugzeiten der Alt- und Jungvögel einerseits sowie der und andererseits erkennen. Altvögel stellen 14,1%, 40,1% der Fänglinge. Anhand der Flügelmaße und Gewichte läßt sich mit fortschreitender Zugzeit keine klinale Variation nachweisen. Ältere Literaturangaben, Helgoland betreffend, werden teils korrigiert, teils präzisiert. Der geringe Anteil der Altvögel bzw. wird auf deren geringer ausgeprägten Zugtrieb zurückgeführt.

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The migration of the sparrow-hawk on Heligoland

Summary On Heligoland the Sparrow-Hawk occurs as a passage visitor only. Mean numbers (17 years) of birds trapped are 0.4 in winter, 2.1 during spring and 23.0 in autumn. Adults and juveniles as males and females as well show different periods of migration. Among birds trapped there are 14.1% adults and 40.1% females. No clinal variation of wing length and weight according to time of passage could be found. Former literature concerning Heligoland is partly corrected, partly rendered more precise. The low proportions of adults and females respectively are caused by weaker migratory urge.

     

Control of the bifunctional O2-sensor kinase NreB of Staphylococcus carnosus by the nitrate sensor NreA: Switching from kinase to phosphatase state

The NreB–NreC two-component system of Staphylococcus carnosus for O₂ sensing cooperates with the accessory nitrate sensor NreA in the NreA–NreB–NreC system for coordinated sensing and regulation of nitrate respiration by O₂ and nitrate. ApoNreA (NreA in the absence of nitrate) interacts with NreB and inhibits NreB autophosphorylation (and activation). NreB contains the phosphatase motif DxxxQ. The present study shows that NreB on its own was inactive for the dephosphorylation of the phosphorylated response regulator NreC (NreC-P), but co-incubation with NreB and NreA stimulated NreC-P dephosphorylation. Either the presence of instead of apoNreA or mutation of the phosphatase motif (D160 or Q164) of NreB abrogated phosphatase activity of NreB. Phosphatase activity was observed for anoxic (active) NreB as well as oxic NreB, therefore the functional state of NreB is not relevant for phosphatase activity. Thus, NreB is a bifunctional sensor kinase with an integral cryptic phosphatase activity. Activation of phosphatase activity and dephosphorylation of NreC-P requires NreA as a cofactor. Accordingly, NreA and nitrate have major and dual roles in NreA–NreB–NreC regulation by (i) inhibiting NreB phosphorylation and (ii) triggering a kinase/phosphatase switch of NreB when present as apoNreA.     

Yaw stability in gliding birds

A new concept for describing the yaw stability in gliding birds is presented. This concept introduces dynamic stiffness in yaw as an appropriate indication of stability. Other than the conventional metric of static yaw stability given by the gradient of the aerodynamic yawing moment with respect to the sideslip angle, the dynamic stiffness does not only provide a qualitative indication of stability but also a precise quantitative measure of the restoring action in the yaw axis. With the use of scaling relations, it is shown that the dynamic stiffness of birds is sufficiently high though their static yaw stability may be very small. The underlying mechanism is that the yaw moment of inertia is more reduced with a decrease in size than the restoring aerodynamic moment. Reference is made to the yaw stability in aircraft and related flying qualities requirements. Thus, numerical values are derived which can be used as a standard of comparison providing a rating basis for the dynamic yaw stiffness in small flying objects, like birds. Furthermore, it is shown that the wings of birds produce yawing moments due to sideslip so large that a sufficiently high level of dynamic yaw stiffness can be achieved. From the results derived in this paper, it may be concluded that birds—unlike aircraft—need no vertical tail for yaw stability.     

Development of a multi-excitation fluorescence (MEF) imaging method to improve the information content of benthic coral reef surveys

Benthic surveys are a key component of monitoring and conservation efforts for coral reefs worldwide. While traditional image-based surveys rely on manual annotation of photographs to characterise benthic composition, automatic image annotation based on computer vision is becoming increasingly common. However, accurate classification of some benthic groups from reflectance images presents a challenge to local ecologists and computers alike. Most coral reef organisms produce one or a combination of fluorescent pigments, such as Green Fluorescent Protein (GFP)-like proteins found in corals, chlorophyll-a found in all photosynthetic organisms, and phycobiliproteins found in red macroalgae, crustose coralline algae (CCA) and cyanobacteria. Building on the potential of these pigments as a target for automatic image annotation, we developed a novel imaging method based on off-the-shelf components to improve classification of coral and other biotic substrates using a multi-excitation fluorescence (MEF) imaging system. We used RGB cameras to image the fluorescence emission of coral and algal pigments stimulated by narrow-waveband blue and green light, and then combined the information into three-channel pseudocolour images. Using a set of a priori rules defined by the relative pixel intensity produced in different channels, the method achieved successful classification of organisms into three categories based on the dominant fluorescent pigment expressed, facilitating discrimination of traditionally problematic groups. This work provides a conceptual foundation for future technological developments that will improve the cost, accuracy and speed of coral reef surveys.

     

Transcriptional Cofactor TBLR1 Controls Lipid Mobilization in White Adipose Tissue

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Highlights? TBLR1 controls cAMP-dependent lipolysis in adipocytes ? Adipocyte-specific deletion of TBLR1 in mice impairs fasting-induced lipolysis ? Lack of TBLR1 in adipocytes aggravates diet-induced obesity and metabolic dysfunction ? TBLR1 mRNA levels in WAT are elevated under lipolytic conditions in mice and humans