Production ecology ofPhragmites communis 1. Relations of two ecotypes to the microclimate and nutrient conditions of habitat

The growth rate of stand biomass, the seasonal development of vertical stand structure and accumulation of mineral nutrients were compared in twoPhrogmites ecotypes; the stands occur in two different biotopes, littoral and limosal, situated in the littoral of the Opatovický fishpond in the South Bohemian fishpond basin. Microclimatological data including incoming global radiation were recorded in both biotopes during three growing seasons. The differences in morphological, chemical and production characteristics of the two reed ecotypes were in good relation with the edaphic, hydrochemical and microclimatological characteristics of their biotopes. These differences are reflected in a higher leaf area index, denser stand, higher production parameters and a higher efficiency in the conversion of solar energy in the limosal reed ecotype as compared with the littoral population. The differences in annual production and in energy conversion have not changed within seven growing seasons.     

Morphological features of F1 generation inRosa hybrids 1. Hybrids of some species of the sect.Caninae withRosa rugosa

In the present paper morphological features of hybrids from crossing of four species ofRosa sect.Caninae (R. canina L.,R. zalana Wiesb.,R. rubiginosa L. andR. sherardii Davies) withR. rugosa Thumbg. (sect.Cinnamomeae) and their heredity are described. F₁ generation appears more or less uniform, certain morphological features are patroclinal, other ones are matroclinal and intermediary. The general appearance of these hybrids is intermediary; there seems to be no reason to consider them matroclinal.     

Participation of exogenous DNA in the repair processes of meristematicVicia faba cells injured by monofunctional alkylating agens ethylmethane sulphonate

The effect of exogenous DNA of syngeneic origin on the course of reparation of meristematic cells ofVicia faba primary roots followed after treatment with monofunctional alkylating agent, ethyl methanesulphonate (EMS), was tested. Time course of alternations in mitotic activity of investigated cellular population and the dynamics of formation of postmetaphase chromosomal aberrations was evaluated. A reparation of damaged cells was significantly supported by syngeneic DNA; its application induced an increased incidence of cellular division already in the early intervals of the repair which was accompanied by concomitant decrease of microscopically detectable rupture in the chromosomes. The study performed on the localization of induced damages occurring in metaphase chromosomes pointed out an increased sensitivity of small chromosomes ofVicia faba to EMS. Similarly, a reparative action of syngeneic DNA was exhibited by significant decrease of aberrations frequency, predominantly in the same chromosomal group. Per cent representation of individual types, not affected by the action of syngeneic DNA, was established by detailed classification of induced aberrations. In both cases, isochromatide breaks were found of greatest predominance.     

Inter- und intrachromosomale Verteilung von Chromatidtranslokationen nach Einwirkung von Trenimon auf menschliche Leukocyten in vitro

250 chromatid interchanges induced by Trenimon were analyzed relative to their configuration, the participation of certain chromosomes or chromosome groups and the localization of the exchange points. Cis- and trans-configuration (=asymmetrical and symmetrical interchanges) have been observed in identical frequency. The same was seen relative to complete and incomplete reunion of the breaks. The interchromosomal as well as the intrachromosomal distribution of the exchange points was non-random. Homologous chromosomes participated in interchanges at a higher level of frequency than expected from their relative length. Chromosomes No. 6–12 and X as well as 16 and 21+22 took part in interchanges more frequently and chromosomes No. 2, 3, 4 and 5 more rarely than expected. The exchange points were frequently observed in the proximal regions of the chromosomes (incl. centromere) as well as in the short arms of chromosomes No. 13–15 and 21+22.     

Immunocytochemical identification of neural elements in the central nervous systems of a snail,some insects,a fish,and a mammal with an antiserum to the molluscan cardio-excitatory tetrapeptide FMRF-amide

Summary The choriocapillaris is the fenestrated capillary network that supplies a large portion of the nutrients required by the retinal pigment epithelium, photoreceptor cells, and other cells of the outer neural retina. The permeability of these capillaries was investigated in the rat by the use of ferritin (mol. wt. approx. 480,000; mol. diam. 110Å) as a tracer. Ninety minutes after intravascular ferritin administration, a high concentration of tracer particles was distributed uniformly in the capillary lumina but few particles were present in Bruch's membrane, the multilayered basement membrane that separates the choriocapillary endothelium from the retinal pigment epithelium. The bulk of the tracer remained in the capillary lumina with a definite blockage seen at fenestral, channel, and vesicle diaphragms. These results indicate that the rat choriocapillary endothelium, unlike the fenestrated endothelia lining other capillary beds, constitutes an important barrier to the passage of ferritin and presumably of circulating native molecules of similar size.Supported by NIH grants EY 01889 and EY 07034 from the National Eye Institute and a grant-in-aid from Fight for Sight, Inc., of New York City     

The spectral input systems of hymenopteran insects and their receptor-based colour vision

Summary Spectral sensitivity functions S() of single photoreceptor cells in 43 different hymenopteran species were measured intracellularly with the fast spectral scan method. The distribution of maximal sensitivity values (_max) shows 3 major peaks at 340 nm, 430 nm and 535 nm and a small peak at 600 nm. Predictions about the colour vision systems of the different hymenopteran species are derived from the spectral sensitivities by application of a receptor model of colour vision and a model of two colour opponent channels. Most of the species have a trichromatic colour vision system. Although the S() functions are quite similar, the predicted colour discriminability curves differ in their relative height of best discriminability in the UV-blue or bluegreen area of the spectrum, indicating that relatively small differences in the S() functions may have considerable effects on colour discriminability. Four of the hymenopteran insects tested contain an additional R-receptor with maximal sensitivity around 600 nm. The R-receptor of the solitary bee Callonychium petuniae is based on a pigment (P596) with a long _max, whereas in the sawfly Tenthredo campestris the G-receptor appears to act as filter to a pigment (P570), shifting its _max value to a longer wavelength and narrowing its bandwidth. Evolutionary and life history constraints (e.g. phylogenetic relatedness, social or solitary life, general or specialized feeding behaviour) appear to have no effect on the S() functions. The only effect is found in UV receptors, for which _max values at longer wavelengths are found in bees flying predominantly within the forest.     

Fermentative conversion of cellulosic substrates to microbial protein byNeurospora sitophila

Neurospora sitophila was used to convert solid cellulosic substrates (sugarcane bagasse, corn stover, wood cellulose) to protein-rich materials for food and fodder. The optimal conversion occurred at 35–37°C and pH 5.5. The fungus was sensitive to excessive agitation; protein production and cellulose utilization were lowered by agitation above 250 rpm in a 75 L fermenter. The cellulolytic capability ofN. sitophila was comparable to that ofChaetomium cellulolyticum, a better known cellulolytic organism.     

The tRNATyr multigene family of Nicotiana rustica: genome organization,sequence analyses and expression in vitro

Tobacco tRNA^Tyr genes are mainly organized as a dispersed multigene family as shown by hybridization with a tRNA^Tyr-specific probe to Southern blots of Eco RI-digested DNA. A Nicotiana genomic library was prepared by Eco RI digestion of nuclear DNA, ligation of the fragments into the vector gtWES·B and in vitro packaging. The phage library was screened with a 5-labelled synthetic oligonucleotide complementary to nucleotides 18 to 37 of cytoplasmic tobacco tRNA^Tyr. Eleven hybridizing Eco RI fragments ranging in size from 1.7 to 7.5 kb were isolated from recombinant lambda phage and subcloned into pUC19 plasmid. Four of the sequenced tRNA^Tyr genes code for the known tobacco tRNA₁ ^Tyr (GA) and seven code for tRNA₂ ^Tyr (GA). The two tRNA species differ in one nucleotide pair at the basis of the TC stem. Only one tRNA^Tyr gene (pNtY5) contains a point mutation (T54A54). Comparison of the intervening sequences reveals that they differ considerably in length and sequence. Maturation of intron-containing pre-tRNAs was studied in HeLa and wheat germ extracts. All pre-tRNAs^Tyr-with one exception-are processed and spliced in both extracts. The tRNA^Tyr gene encoded by pNtY5 is transcribed efficiently in HeLa extract but processing of the pre-tRNA is impaired.     

Regulation of the Bacillus subtilis W23 xylose utilization operon : interaction of the Xyl repressor with the xyl operator and the inducer xylose

Summary A crude protein extract of Bacillus subtilis W23 contains a sequence-specific DNA binding activity for the xyl operator as detected by the gel mobility shift assay. A xylR determinant encoded on a multicopy plasmid leads to increased expression of this binding activity. In situ footprinting analysis of the protein-DNA complex in a polyacrylamide gel shows that the xyl operator is sequence-specifically bound and protected from cleavage by copper-phenanthroline at 26 phosphodiester bonds on each strand. Quantitative competition assays for repressor binding reveal that a 25 by synthetic xyl operator cloned into a polylinker is bound with the same affinity as the operator in the wild-type xyl regulatory region. This confirms that no additional sites in the wild-type sequence contribute to repressor binding. The xyl operator consists of ten palindromic base pairs flanking five central non-palindromic base pairs. A mutational analysis shows that the sequence of the central base pairs contributes to recognition by the repressor protein and that the spacing of the palindromic elements is crucial for repressor binding. An operator half site is not bound by the repressor. In vivo and in vitro induction studies suggest that, of several structurally similar sugars, xylose is the only molecular inducer of the Xyl repressor.     

Biofilm community structure and the associated drag penalties of a groomed fouling release ship hull coating

Grooming is a proactive method to keep a ship’s hull free of fouling. This approach uses a frequent and gentle wiping of the hull surface to prevent the recruitment of fouling organisms. A study was designed to compare the community composition and the drag associated with biofilms formed on a groomed and ungroomed fouling release coating. The groomed biofilms were dominated by members of the Gammaproteobacteria and Alphaproteobacteria as well the diatoms Navicula, Gomphonemopsis, Cocconeis, and Amphora. Ungroomed biofilms were characterized by Phyllobacteriaceae, Xenococcaceae, Rhodobacteraceae, and the pennate diatoms Cyclophora, Cocconeis, and Amphora. The drag forces associated with a groomed biofilm (0.75 ± 0.09 N) were significantly less than the ungroomed biofilm (1.09 ± 0.06 N). Knowledge gained from this study has helped the design of additional testing which will improve grooming tool design, minimizing the growth of biofilms and thus lowering the frictional drag forces associated with groomed surfaces.