Mechanism of Kasugamycin Resistance in <Emphasis Type="Italic">Escherichia coli</Emphasis>

Strains of Escherichia coli are resistant to the antibiotic kasugamycin due to the partial non-methylation of 16S ribosomal RNA. An RNA methylase activity, absent from resistant strains, is shown here to methylate in vitro the 16S RNA of resistant as well as sensitive strains.     

Developmental Physiology of Sugar Beet: I. THE INFLUENCE OF LIGHT AND TEMPERATURE ON GROWTH

Sugar beet plants were grown for 12 weeks from emergence ingrowth rooms at temperatures of 10, 17, 24 and 31 °C and20, 50, 80, and 110 cal visible radiation cm^-2d^-1, and the changeswith time in their dry weight, leaf area, leaf numbers, andstorage root sugar determined. The first stage of growth wasdominated by the development of the shoot, but the storage rootgradually assumed increasing importance and eventually grewat a faster rate and to a greater weight than the shoot. Therelative growth rate and final yield of dry matter of the shootwere greatest at 24 °C and of the root between 17 and 24°C. The relative rate of expansion and the final area ofthe leaf surface were also greatest at 24 °C, whilst therates of production and of unfolding of leaves were greatestat about 17 °C. All these attributes were increased withincreased radiation. Net assimilation rate increased almostproportionately with radiation and was not significantly affectedby temperature.The relationships of total leaf area with plantdry weight, root dry weight with shoot dry weight, and totalleaf number with plant dry weight were scarcely affected bychanges in radiation, but were much influenced by temperature.Plants of the same dry weight generally had bigger roots andsmaller areas of leaf surface as temperatures departed from24 °C and had most leaves at 17 °C. Sugar concentrationsin the storage root were greatest at 17 °C, but the totalamount of sugar was about the same at 17 and 24 °C. Theconcentration of sugar in the storage root depended on rootsize.Thus, temperature affected both the rate and pattern ofdevelopment, and radiation affected the rate but not the patternof development.     

Phylogeny of the tribe Sciophilini (Diptera: Mycetophilidae: Sciophilinae)

The monophyly and phylogenetic relationships within the species rich Sciophilini (Diptera: Mycetophilidae) were analysed, based on 96 adult morphological characters. The cladistic analysis included 80 Sciophilini exemplar species (representing all but 1 of the 36 genera placed previously in the Sciophilini) and 11 outgroup taxa of other mycetophilid tribes. The monophyly of Sciophilini was supported in the parsimony analysis by four synapomorphies. The tribe now contains 34 genera: Acnemia Winnertz, Acomoptera Vockeroth, Adicroneura Vockeroth, Afrocnemia Matile, Allocotocera Mik, Anaclileia Meunier, Aneura Marshall, Austrosciophila Tonnoir, Azana Walker, Baeopterogyna Vockeroth, Cluzobra Edwards, Drepanocercus Vockeroth, Duretophragma Borkent gen.n. , Eudicrana Loew, Leptomorphus Curtis, Loicia Vockeroth, Megalopelma Enderlein, Monoclona Mik, Morganiella Tonnoir & Edwards, Neoallocotocera Tonnoir, Neoaphelomera Miller, Neotrizygia Tonnoir & Edwards, Neuratelia Rondani, Paramorganiella Tonnoir, Paratinia Mik, Paratrizygia Tonnoir, Parvicellula Marshall, Phthinia Winnertz, Polylepta Winnertz, Sciophila Meigen, Stenophragma Skuse, Tasmanina Tonnoir, Taxicnemis Tonnoir & Edwards, and Trizygia Skuse. Four genera placed previously in Sciophilini (Coelophthinia Edwards, Impleta Plassmann, Speolepta Edwards and Syntemna Winnertz) are transferred to the Gnoristini. Neoneurotelia Shinji and Neoparatinia Shinji are considered nomina dubia . Diagnoses are given for all genera in the tribe. Duretophragma gen.n. is described for the following species (all of which are comb.n. ): Duretophragma andina (Duret), Duretophragma argentina (Duret), Duretophragma glabanum (Johannsen), Duretophragma fusca (Edwards), Duretophragma humeralis (Edwards), Duretophragma intermedia (Edwards), Duretophragma longifurcata (Freeman) (type species), Duretophragma morigenea (Edwards), Duretophragma naumanni (Duret), Duretophragma nigricauda (Edwards), Duretophragma obscura (Duret), Duretophragma ochracea (Freeman), Duretophragma pleuralis (Edwards) and Duretophragma similis (Johannsen). Other new generic combinations include: Trizygia albidens (Oliveira & Amorim) comb.n. , Trizygia alvesi (Oliveira & Amorim) comb.n. , Trizygia balbi (Oliveira & Amorim) comb.n. , Trizygia camargoi (Oliveira & Amorim) comb.n. and Afrocnemia stellamicans (Chandler) comb.n .     

Developmental manipulation of the circadian pacemaker in the cockroach: relationship between pacemaker period and response to light

Abstract Previous research has shown that fundamental properties of the circadian pacemaker that drives the rhythm of locomotor activity in the cockroach Leucophaea maderae L. are permanently altered by exposure of animals to 22 or 26 h light cycles during post-embryonic development (Barrett & Page, 1989; Page & Barrett, 1989). The present results document differences between animals exposed to either constant darkness (DD) or constant light (LL) during postembryonic development in the free-running period, the phase shifting response to light pulses, and the response to an LL to DD transition of the adult pacemaker. In addition, the changes in pacemaker period and in the phase shifting response that result from raising animals in several different lighting conditions are shown to be strongly correlated. The data suggest there is a developmentally labile interdependence between the period of the pacemaker and its sensitivity to light.     

Error in the inference of fire history from grasstrees

Abstract A method for constructing fire histories has recently been proposed for fire‐prone southern Australia based on the pattern of coloured bands in the remnant leaf‐bases on stems of grasstrees (Xanthorrhoea species; Xanthorrhoeaceae). In the absence of alternative high‐resolution techniques extending into the premodern period, this method has been utilized to construct fire histories for forest, woodland and shrubland ecosystems, principally in south‐western Australia. However, the technique has not been validated against known fire histories spanning more than one fire interval. Here we compare fire records from 100 grasstrees with a 30‐year record (1973–2002) of fire data derived from satellite imagery in a region of sandplain shrubland vegetation near Eneabba in south‐western Australia. Fires occurred in eight of the 30 years of the satellite record, with sampled grasstrees burning between zero and four times. The grasstree and satellite records agreed in terms of the overall incidence of fires experienced over the 30‐year period, with the grasstree record matching the satellite record significantly better than chance. However, comparison of the grasstree and satellite records found substantial error in the rate of both false positives and false negatives. Grasstrees failed to identify fire in 83% of fire occurrences identified by the satellite record, down to 53% if an error of ±2 years in the attribution of year of fire was allowed. A similar proportion of grasstree fire incidents were not matched in the satellite record (false positives). The rate of false positives increased with time before present, suggesting a temporal bias in the grasstree record. It is clear that the grasstree record does reflect fire history to a degree, but that it contains at least as many false as true fire records and may tend towards over‐reporting the incidence of fire in the past.     

Diurnal cycles of leaf extension in unsalinized and salinized Beta vulgaris

Abstract. Continuous high resolution measurement of sugar beet leaf extension over 5 d in growth chambers showed average leaf extension rates (LER) in darkness to be from three to six times those in light for plants growing in non-salinized media. The changes in LER in light-dark transitions occurred within seconds, a response which was more rapid than stomatal opening or closing. When the growth medium was salinized to 100 mol m⁻³ NaCl, LER's were reduced by about 50% in darkness and 90% in light, markedly increasing the ratio of dark to light LER.
A 2-d episode of root-zone salinity imposed midway through a 5-d period of measurement decreased LER and produced higher leaf temperatures. LER and diurnal leaf temperature patterns reverted to their pre-salinized levels when root-zone salinity was removed. Thus, the effects of short episodes of high sodium chloride in the growth medium appear to be reversible, suggesting a water stress mechanism of growth reduction rather than toxicity effects of salt.     

Effects of enhanced ultraviolet radiation and carbon dioxide concentration on the moss Hylocomium splendens

In a laboratory experiment interaction effects of UV-B and CO₂ on photosynthesis and growth of the moss Hylocomium splendens were studied. The plants were exposed to two CO₂ levels (350 ppm and 600 ppm) and three UV-B levels (no UV-B, ambient UV-B and that corresponding to 20% ozone depletion) for 5 months. The effects were recorded by measuring the photosynthetic response and growth of the plants. There was a statistically significant change in photosynthetic efficiency and maximum photosynthetic rates due to time and to enhanced CO₂ concentration, whereas there was no effect due to UV-B. There was a decreased growth due to both UV-B and CO₂ and an interaction effect on growth (in length). The UV-B dose corresponding to the ambient level had a larger reducing effect on growth than the highest UV-B dose. This was a counter-intuitive result and the following tentative interpretation was made: differences in the measured UV-A/UV-B/PAR ratios between the treatments could explain the result provided there was a non-linear response to UV over the range of irradiance levels used.     

Relationship between Electrical Resistance and Capacitance of Wood in Progressive Stages of Discoloration and Decay

Electrical resistance and capacitance measurements were madeon woody tissues of several tree species. Each tissue was abovethe fibre-saturation point. Values of capacitance were inverselyproportional to values of resistance in woody tissues in progressivestages of discoloration and decay. With the electrode separationused, clear woody tissues had resistances of 110 to 30 k andcapacitances of 0·002 to 0·110 µF. Resistanceand capacitance measure ments of discoloured tissues were 29to 8 k and 0·005 to 0·040 µF, respectively,and those of decayed tissues were 5 to 1 k and 0·60 to0·110 µF. Either electrical measurement could beused to measure the stages of deterioration in woody tissues.Ground woody tissues, cellulose suspensions, starch suspensions,and wood equivalent solutions of potassium chloride had resistanceand capacitance properties similar to those found in intactwoody tissues. Electrical resistance and capacitance propertiesof woody tissues above the fibre-saturation point appear tobe similar to those of dilute solutions of mobile ions.     

SENSORY THRESHOLDS: ESTIMATION FROM DOSE-RESPONSE CURVES

Three methods of threshold estimation are compared for the detection of 1,8-cineole added to Concord grape juice presented in a semi-ascending paired difference design (Lundahl et al. 1986). Method A tests the significance of obtaining a nonzero response, method B determines the transition point of a 2-phase linear model fitted to the data, method C fits a logistic model to the data and defines threshold as the point of maximum curvature, C_max, of the curve. Method A yields interval estimates of thresholds, the midpoints of which systematically decrease with increasing sample size. Methods B and C yield point estimates of thresholds which do not systematically decrease with increasing sample size, are a feature of the dose-response curve, and are similar in value to each other.