Über die Anwendung des Raster-Elektronenmikroskopes in der Holzanatomie

Summary With regard to its great depth of focus and the very good disintegration the Stereoscan-electron-microscope allows to take a new way in the exploration of cell wall structure and pits as in some examples is demonstrated here.     

Mining functional information associated with expression arrays

Deciphering the networks of interactions between molecules in biological systems has gained momentum with the monitoring of gene expression patterns at the genomic scale. Expression array experiments provide vast amounts of experimental data about these networks, the analysis of which requires new computational methods. In particular, issues related to the extraction of biological information are key for the end users. We propose here a strategy, implemented in a system called GEISHA (gene expression information system for human analysis) and able to detect biological terms significantly associated to different gene expression clusters by mining collections of Medline abstracts. GEISHA is based on a comparison of the frequency of abstracts linked to different gene clusters and containing a given term. Interpretation by the end user of the biological meaning of the terms is facilitated by embedding them in the corresponding significant sentences and abstracts and by establishing relations with other, equally significant terms. The information provided by GEISHA for the available yeast expression data compares favorably with the functional annotations provided by human experts, demonstrating the potential value of GEISHA as an assistant for the analysis of expression array experiments. Electronic Publication     

Differential effect of antiepileptic and non-antiepileptic drugs on the reticular formation

The effect of the antiepileptic drugs carbamazepine and phenytoin, and of the non-antiepileptic drug baclofen, was compared on various inhibitory and excitatory mechanisms in the feline trigeminal nucleus. Baclofen resembled carbamazepine and phenytoin in depressing segmental excitatory and facilitating segmental inhibitory mechanisms. However, baclofen facilitated the periventricular and periaqueductal inhibition of the trigeminal nucleus, while carbamazepine and phenytoin depressed these descending inhibitory mechanisms. Baclofen also resembles carbamazepine and phenytoin in its effectiveness in trigeminal neuralgia, but baclofen is not a clinically effective antiepileptic agent. Our experiments indicate that the ability to depress the reticular formation of the diencephalon and midbrain is an important characteristic of antiepileptic drugs. This suggests that the reticular core is involved in the spread and generalization of seizures.     

Statistical and Economic Techniques for Site-specific Nematode Management

Recent advances in precision agriculture technologies and spatial statistics allow realistic, site-specific estimation of nematode damage to field crops and provide a platform for the site-specific delivery of nematicides within individual fields. This paper reviews the spatial statistical techniques that model correlations among neighboring observations and develop a spatial economic analysis to determine the potential of site-specific nematicide application. The spatial econometric methodology applied in the context of site-specific crop yield response contributes to closing the gap between data analysis and realistic site-specific nematicide recommendations and helps to provide a practical method of site-specifically controlling nematodes.     

Configuron dependence on translation of specific condon pairs. I. Helical regions of human alpha and beta globins

Homologous proteins, which possess similar shapes, functions, and amino acid sequences, are encoded by homologous messenger ribonucleic acids whose codon sequences tend to be similar. It is proposed that helical configurons are generated when certain pairs of contigous codons are translated, and that non-helical configurons appear when other specific pairs of codons are read off. The resulting sequence of configurons comprises the polyconfiguron, which forms the native structure of the protein.     

ELECTRON MICROSCOPY OF PHIALIDES AND CONIDIOGENESIS IN TRICHODERMA SATURNISPORUM

Each phialide had a thick-walled neck region located immediately below a light microscopically inconspicuous collarette. The thickened wall of the phialide neck was multilaminate, with layers of different electron transmission properties. A developmental stage in the formation of the first conidial initial was observed. Conidial initials blew out through the thickened neck region, increased in size, and were eventually delimited by centripetally developing septa. Mature, winged conidia had an electron-opaque outer wall layer and an electron-transparent inner wall layer. The wing was formed by separation of these outer and inner wall layers and buckling or wrinkling of the outer layer. As early as they could be discerned, conidial initials had developed the electron-opaque wall layer which characterized mature conidia. Each conidium-delimiting septum became bilayered; the upper layer formed part of the conidial base, and the lower layer became a portion of the wall of the next conidial initial. Phialides lacked an electron-opaque wall layer, and they possessed areas of abundant rough endoplasmic reticulum, as well as free ribosomes. Lipid globules were also abundant, especially in conidia. The distinction between phialides and annellides was questioned.     

A molecular phylogeny of the Cephalaspidea sensu lato (Gastropoda: Euthyneura): Architectibranchia redefined and Runcinacea reinstated

The monophyly and phylogenetic relationships of the Cephalaspidea sensu lato ( sensu   Burn and Thompson 1998 ) have been investigated by means of Bayesian, parsimony and distance analyses of nuclear (18S rRNA and 28S rRNA) and mitochondrial cytochrome oxidase I (COI) genes.
Results revealed the presence of three monophyletic groups among the Cephalaspidea s. l. (i) Architectibranchia ( sensu   Haszprunar 1985 , in part: including Acteonidae and Aplustridae, but excluding Diaphanidae), (ii) Cephalaspidea including Diaphanidae but not Runcinidae (both previously of uncertain systematic affinity), and (iii) Runcinacea.
The monophyly of the architectibranch families Acteonidae (represented by Acteon and Pupa ) and Aplustridae ( Hydatina and Micromelo ); of the runcinacean family Runcinidae ( Runcina ); and of the cephalaspidean families Aglajidae ( Chelidonura , Aglaja , Odontoglaja , Navanax and Philinopsis ), Bullidae ( Bulla ), Gastropteridae ( Siphopteron and Sagaminopteron ), Haminoeidae ( Atys , Haminoea , Phanerophthalmus and Smaragdinella, but not Ventomnestia ), and Retusidae ( Retusa and Pyrunculus , but not Volvulella ) is suggested. The families Scaphandridae ( Scaphander ) and Rhizoridae ( Volvulella ) are reinstated as valid. A new phylogenetic classification of the Cephalaspidea is proposed.     

Preparative and analytical separation of the zopiclone enantiomers and determination of their affinity to the benzodiazepine receptor binding site

We report the preparative separation of rac-zopiclone using malic acid as the resolving agent. Furthermore, two different methods for the analytical determination of zopiclone enantiomers by HPLC on chiral stationary phases are described. The benzodiazepine receptor binding of the isolated enantiomers was investigated. Half-maximal inhibitory concentrations of (+)- and (?)-zopiclone were 21 or 1,130 nmol/liter, respectively, indicating a more than 50 times higher affinity of the (+)-enantiomer toward the receptor. © 1993 Wiley-Liss, Inc.     

Detection of a Single-Locus Gene on Channel Catfish Chromosomes by In-Situ Polymerase Chain Reaction

An in-situ polymerase chain reaction (ISPCR) procedure was applied to chromosomal localization of the gene, Ig H, encoding the immunoglobulin heavy chain of channel catfish (Ictalurus punctatus). Metaphase chromosomes were prepared by a replication banding procedure and subjected to ISPCR using biotin-labeled primers. The hybridization signals were detected with an avidin-fluorescein isothiocyanate (FITC)-based method, and chromosome bands revealed by simultaneous or sequential treatment methods. Standard fluorescent in-situ hybridization (FISH) was performed on chromosome preparations to compare with the ISPCR procedure. The Ig H gene was detected at the telomeric position of a chromosome with a relative length of 3.2 ± 0.2%. The Ig H-bearing chromosome detected by the FISH method was identical to that found by ISPCR procedure. Visibility of chromosome bands was reduced by heat and salt treatments and could not be analyzed after thermocycling. Therefore, specific identity of the chromosome bearing the Ig H gene remains unknown. Banding of fish chromosomes is difficult and poses a barrier for applying current molecular techniques to physical mapping of teleost genomes. Application of the ISPCR to chromosomal mapping is new for fish species and is only in initial stages of development for higher vertebrates.