Habitat preferences of some red‐listed alpine plants in Scandinavia

Scandinavian alpine vascular plants are red‐listed (R‐L) according to criteria defined by IUCN. These are based on an evaluation of their risk for extinction in the future, which for most alpine plants have been related to possible effects of climate change. In the present study, ecological characteristics of R‐L alpine plants are inferred from their occurrence in previously studied alpine plant communities. In total, data on 231 communities were compiled from studies in Norway and Sweden, and a total of 39 red‐listed vascular plants were found in 142 of them. The data were analysed by numerical analyses in order to assess if and how communities with and without R‐L species differ in terms of floristic composition and environmental conditions. The analysies show that most of the R‐L plants are situated at the ends of the main floristic gradients extracted by Detrended Correspondense Analysis (DCA). These extremes are interpreted to represent high‐altitudinal communities with long‐lasting snow cover. In productive communities dominated with herbs and ferns, R‐L plants are few or missing. A Principal Components Analysis (PCA) indicated that the R‐L species form a heterogeneous group both in terms of ecology, abundance, and geographic distribution. Some of the communities were considered to be especially valuable because they included several (up to eight) R‐L plants. Such communities are found in the upper part of the middle alpine or high alpine zone (460–675 m above the forest limit) and on calcareous substrate. It may generally be assumed that alpine plants with optima at the edges of the floristic gradients may be especially vulnerable to climate changes.     

Cloning and characterization of two plasmids from Bacillus thuringiensis in Bacillus subtilis

Bacillus thuringiensis subspecies israliensis plasmids pTX14-1 and pTX14-3 were cloned and analyzed by Southern blot hybridization for their replication mechanism in Bacillus subtilis. The cloning of pTX14-1 into the replicon deficient vector pBOE335 showed the usual characteristics of single-stranded DNA plasmids, i.e., it generated circular single-stranded DNA and high molecular weight (HMW) multimers. The other plasmid, pTX14-3, behaved differently; it generated neither single-stranded DNA nor HMW multimers. Treatment with rifampicin did not result in the accumulation of single-stranded DNA. However, deletion of an EcoRI-PstI fragment resulted in the accumulation of both single-stranded DNA and HMW multimers. From various deletion derivatives, we have mapped the minus origin and the locus responsible for suppression of HMW multimer formation. Full activity of the minus origin and of the locus suppressing HMW formation was only observed on the native replicon, indicating a coupling to the plus strand synthesis.     

Mechanism of postsegregational killing by the hok gene product of the parB system of plasmid R1 and its homology with the relF gene product of the E. coli relB operon.

The parB region of plasmid R1 encodes two genes, hok and sok, which are required for the plasmid-stabilizing activity exerted by parB. The hok gene encodes a potent cell-killing factor, and it is regulated by the sok gene product such that cells losing a parB-carrying plasmid during cell division are rapidly killed. Coinciding with death of the host cell, a characteristic change in morphology is observed. Here we show that the killing factor encoded by the hok gene is a membrane-associated polypeptide of 52 amino acids. A gene located in the Escherichia coli relB operon, designated relF, is shown to be homologous to the hok gene. The relF gene codes for a polypeptide of 51 amino acids, which is 40% homologous to the hok gene product. Induced overexpression of the hok and relF gene products results in the same phenomena: loss of cell membrane potential, arrest of respiration, death of the host cell and change in cell morphology. The parB region and the relB genes were cloned into unstably inherited oriC minichromosomes. Whereas the parB region also conferred a high degree of genetic stability to an oriC minichromosome, the relB operon (with relF) did not; therefore the latter does not appear to 'stabilize' its replicon (the chromosome). The function of the relF gene is not known.     

Estimation of Plasmid Loss Rates in Bacterial Populations with a Reference to the Reproducibility of Stability Experiments

Two methods for estimation of plasmid loss rates were tested on data obtained from traditional (serial transfer) stability experiments. The first method was based on the assumption that the plasmid does not inhibit the growth of its host, whereas the second method takes differences in the interdivision time of plasmid-free and plasmid-carrying cells into account. In the cases where the loss rate is high and the plasmid does not exert strong growth inhibition, the estimates appear very reliable. When the plasmid loss rate is small and the plasmid exerts inhibition of growth to its host, the experimental design becomes unreliable.     

Effect of Organic Acids on Reactions Catalyzed by Manganese Peroxidase from Phanerochaete chrysosporium

The effect of several organic acids on the oxidation of Mn(II) catalyzed by manganese peroxidase was studied. Reactivities of manganese peroxidase and chemically prepared Mn(III) organic acid complexes towards phenolic compounds were compared. If lactate appears to be the best complexant for manganese peroxidase activity, chemically prepared Mn(III)—lactate complex is a less effective oxidant towards phenolic compounds than other Mn(III)—complexes. Our results agree with the hypothesis that certain organic acids are involved in the catalytic cycle of manganese peroxidase. Malonate and lactate seem to be the most attractive complexants for practical applications of manganese peroxidase and were used in enzymatic treatment of hardwood kraft pulp. Bleaching of kraft pulp was studied and after alkaline extraction, a significant decrease of kappa number was measured. The bleaching was enhanced in lactate buffer.     

Frond development and phenology of Thelypteris limbosperma, Athyrium distentifolium, and Matteuccia struthiopteris in Western Norway

Odland, A. 1995. Frond development and phenology of Thelypteris limbosperma, Athyrium distentifolium, and Matteuccia struthiopteris in Western Norway. — Nord. J. Bot. 15: 225–236. Copenhagen. ISSN 0107–055X. The pattern of growth and phenology of Thelypteris limbosperma, Athyrium distentifolium, and Matteuccia struthiopteris fronds has been investigated, with particular emphasis on height increments of the sporophytes and the development of fertile fronds. In order to study both interspecific and intraspecific differences, fern stands along altitudinal gradients have been monitored. To investigate the initiation of fertility, fronds representing different developmental stages have been sampled. Climatic data have been collected with a data-logger during the study periods. The ferns show significant differences in growth pattern and phenology. Matteuccia struthiopteris has a growth curve that is best described as monomolecular, characterised by high growth rates during the early developmental stage, while the development of Thelypteris limbosperma and Athyrium distentifolium follow a logistic growth curve. The species need different periods of time to develop their fronds. The main frond elongation does not start before soil temperature has reached 7 C. After that, the growth is mainly controlled by air temperature. Within the interval when mean maximum temperatures are 8–20 C, all three ferns showed increased growth rates with increasing air temperatures, but the increase was greatest in M. struthiopteris. At higher temperatures, the growth rate of M. struthiopteris and T. limbosperma decreased. Athyrium distentifolium is characterised by producing sori at an early developmental stage. Fertile Matteuccia strurhiopteris fronds are developed at a much later developmental stage. Thelypteris limbosperma needs a longer period of time to produce mature fronds than the other species. The investigation indicates that plant growth and development are determined by both internal and external factors. It is concluded that growth rate, phenology, and the ability of ferns to produce mature fronds reveal close similarities with their response to environmental variables, and hence with their broad-scale geographical distributional patterns.     

Study of pH and temperature-induced transitions in urate oxidase (Uox-EC1.7.3.3) by microcalorimetry (DSC), size exclusion chromatography (SEC) and enzymatic activity experiments

Purified recombinant urate oxidase (urate oxygen oxidoreductase EC 1.7.3.3. re-Uox) has been studied by means of differential scanning calorimetry (DSC) in correlation with enzymatic activity measurements and size exclusion chromatography. Differential scanning calorimetry curves versus pH show two endothermal effects in the pH range 6-10. The first endotherm reveals a maximum stability between pH 7.25 and pH 9.5 corresponding to a temperature of transition T(m1) of 49.0 degrees C and an enthalpy of transition of 326 kJ mol(-1). This value dramatically decreases below pH 7.25. The behavior of the second endotherm is more complex but the temperature of transition T(m2) is constant between pH 9 and 7.25 and a maximum for the corresponding enthalpy is obtained near pH 8 with DeltaH(2)=272 kJ mol(-1). An optimal pH of 8.0 for the stability of the enzymatic activity at elevated temperature was also found which was in good agreement with calorimetric results. Reversibility of the first endotherm is obtained from 20 to 51.5 degrees C. The calorimetric result is correlated to enzymatic activity, purity by size exclusion chromatography (SEC) and protein concentration measurements. In contrast, for the second endotherm, after heating up to 68.9 degrees C, no reversibility was found. Interaction with structural analogues of urate has been studied by DSC. 8-Azahyooxanthine has only a small effect and caffeine has no effect at all. With 8-azaxanthine, a rapid increase of the T(m1) function of the concentration is obtained. At high concentration T(m1) reached the T(m2) value which remained unaffected.     

Neue diterpene und germacranolide aus Mikania-Arten

From three Mikania species, three new labdanic acid and two kaurenic acid derivatives have been isolated together with known compounds and four new germacranolides, differing only in the ester moiety.     

Cell counting and carbon utilization velocities via microbial calorimetry

Bacteria rapidly metabolize sugars and produce heat accordingly (Escherichia coli, aerobic conditions, 25 degrees C). Two kinds of heat output are gotten: (1) from excess cells and limiting carbon, 2 x 10(9) to 5 x 10(9) cells, 5-50 nanomole glucose; (2) from limited cells and excess carbon, 0. 1 x 10(9)-1 x 10(9) bacteria and 200-600 nmol glucose. The thermograms from heat conduction calorimetry under the first conditions measure velocities of sugar uptake and initial metabolic throughput in 1-6-min time spans before a growth cycle possibly can occur. Under the second conditions with limited cells, power output plateaus to a steady state proportional to cell biomass and number of cells. In order to evaluate the calorimetric means for measuring number of cells, six independent means including spectrophotometry (turbidity) were compared: microkjeldahl nitrogen, biuret protein, dry weight, microscopy direct counting in Petroff-Hausser chambers, and viable colony counting. Using turbidity as a central standard, all methods including calorimetry under the second set of conditions agree within +/-18% of one another. Spectrophotometry is the most rapid method but is seriously interfered with by pigments that absorb and foreign particles that also scatter. Calorimetry requires 10-30 min but measures cell numbers in opaque samples impossible for optical means.     

What Is Secondary about Secondary Tropical Forest? Rethinking Forest Landscapes

Forests have long been locations of contestation between people and state bureaucracies, and among the knowledge frameworks of local users, foresters, ecologists, and conservationists. An essential framing of the debate has been between the categories of primary and secondary forest. In this introduction to a collection of papers that address the questions of what basis, in what sense, and for whom primary forest is ‘primary’ and secondary forest is ‘secondary,’ and whether these are useful distinctions, we outline this debate and propose a new conceptual model that departs from the simple binary of primary and secondary forests. Rather, we propose that attention should be given to the nature of the disturbance that may alter forest ecology, the forms of regeneration that follow, and the governance context within which this takes place.