Constituents of the stem bark of Ormosia wayana.

The isolation of lupeol, beta-sitosterol acetate and three quinolizidinic alkaloids, (+)-lupanine, (-)-sparteine and (-)-3 beta-hydroxy-13 alpha-tigloyloxy-lupanine (1), from the stem bark of Ormosia wayana is reported.     

48. Deutsche Weltkongreß und Internationale Weinbauausstellung

Ohne Zusammenfassung     

A carbon balance model of peach tree growth and development for studying the pruning response

We modeled tree responses to pruning on the basis of growth rules established on unpruned trees and a simple principle governing root-shoot interactions. The model, which integrates architectural and ecophysiological approaches, distinguishes four types of anatomical organs in a tree: rootstock, main axis, secondary axes and new roots. Tree structure is described by the position of secondary axes on the main axis. The main processes considered are plastochronal activity, branching, assimilate production, respiration and assimilate partitioning. Growth and development rules were based on measurements of two unpruned trees. The model was used to simulate growth of peach trees (Prunus persica (L.) Batsch) in their first growing season. Assuming that the equilibrium between roots and shoots tends to be restored after pruning, the response to removal of the main axis above the twentieth internode in mid-July was simulated and compared to the response measured in three pruned trees. The model fit the unpruned tree data reasonably well and predicted the main traits of tree behavior after pruning. Dry matter growth of the secondary axes of pruned trees was increased so that shoot seasonal carbon balance was hardly modified by pruning. Rhythmicity of growth was enhanced by pruning, and might result from variations induced in the root:shoot ratio. Variation in pruning severity had greater effects than variation in pruning date. A sensitivity analysis indicated that: (1) root-shoot partitioning was a critical process of the model; (2) tree growth was mainly dependent on assimilate availability; and (3) tree shape was highly dependent on the branching process.     

Some biological interactions between the parasitoid <Emphasis Type="Italic">Anagyrus pseudococci</Emphasis> (Girault) (Hymenoptera: Encyrtidae) and its host <Emphasis Type="Italic">Planococcus ficus</Emphasis> (Signoret) (Hemiptera: Coccoidea: Pseudococcidae)

The development, longevity, fecundity and life-table parameters of the endoparasitoid Anagyrus pseudococci (Girault) (Hymenoptera: Encyrtidae), 15 d.o. (3rd-instar nymphs) and 21 d.o. (young adult females) of the vine mealybug, Planococcus ficus (Signoret) (Hemiptera: Pseudococcidae) at 28 ± 1°C, 65 ± 10%RH and 16:8h L:D under laboratory conditions. The developmental time of female parasitoids within the host was 17.7 ± 0.39 days in 15 d.o. and 16.65 ± 0.25 days in 21 d.o. hosts; for males, development time was 16.85 ± 0.29 and 15.25 ± 0.09 days, respectively. The average number of offspring per female was 22.35 ± 1.68 in 15 d.o. and 34.8 ± 2.56 in 21 d.o. vine mealybugs. The longevity of female parasitoids was 14.8 ± 0.98 days in 15 d.o. and 15.65 ± 0.92 days in 21 d.o. mealybugs, respectively; for males, longevity was determined as 7.3 ± 0.43 and 6.7 ± 0.54 days, respectively. The mean time of pupation was 7.85 ± 0.003 days in 15 d.o. mealybugs and 8.65 ± 0.003 days in 21 d.o. mealybugs. The aggregate encapsulation rate in the parasitized 15 d.o. mealybugs was 49.73 and 60.36% in 21 d.o. mealybugs. Furthermore, effective encapsulation was 24.82% in 15 d.o. mealybugs and 37.50% in 21 d.o. mealybugs. Population growth rate (r _m) for A. pseudococci was 0.0999 female/female/days in 15 d.o. mealybugs and 0.1269 female/female/days in 21 d.o. mealybugs. The mean population generation time was 23.49 days for parasitoids reared in 15-days-old and 22.39 days when reared in 21 d.o. mealybugs.     

Edge effects and forest water use: A field study in a mixed deciduous woodland

A field study was carried out in a mixed deciduous forest in order to measure the spatial variability of evapotranspiration in relation to distance from the nearest forest edge. Throughfall was collected in storage gauges in a transect across the edge. Transpiration was measured at the tree scale by means of the sap flux technique. Thermal dissipation probes were inserted into the hydro-active sapwood of 12–16 sample trees at a time covering four species. The sample trees were located close to a north- and a south-facing forest edge and between 3 and 69 m away from the nearest edge. The probes were moved to new trees about once a month and in total 71 trees were sampled. Sap flux densities were compared with potential evaporation and scaled up to the stand through multiplication with sapwood area per unit ground area. No significant edge effect on interception evaporation could be detected but there was a large influence on stand transpiration which increased towards the edge. In ash (Fraxinus excelsior L.), this increase resulted mainly from enhanced sap flux density (by 33–82%, depending on the size class) in trees located at the edge, whereas in oak (Quercus robur L.) the sap flux density was similar in edge and inner trees and an effect was only found at the stand scale in the way that the total basal area, per unit ground area, was larger near the forest edge than in the forest interior. Hawthorn (Crataegus monogyna L.) and field maple (Acer campestre L.), which occurred mainly in the understorey, were only weakly affected by the proximity to an edge. At the stand scale the total seasonal transpiration varied between 354 mm in the forest interior (>45 m away from the edge) and 565 mm at the forest edge (<15 m away from the edge), whilst the potential evaporation over the same period was 571 mm. This corresponds to Priestley–Taylor coefficients of 0.78 in the interior and 1.25 at the edge, whilst intermediate numbers were found for the area between the edge and inner zones. Using these results to calculate the average water loss per unit ground area of hypothetical woodlands of various sizes, it is shown that the edge effect dominates the water use of small forests and becomes negligible only for woodlands larger than 100 ha.     

Regional differences in harvesting levels and wood-based employment in Norway

In this paper, a statistical framework based upon shift-share analysis is employed to analyse regional differences in Norway regarding changes in harvesting levels and number of full-time equivalent employees in wood processing. Changes in harvesting levels and employment differ between regions. A tendency found is that there has been a moderate centralisation in the period 1990–2000 with respect to harvesting levels. The analysis indicates that remote municipalities harvest relatively more in periods with a high harvesting intensity, while the harvesting level is more evenly distributed among the regions in other periods. There is, however, no clear picture whether there has been a centralisation or decentralisation regarding woodbased employment. Differences between regions may therefore be explained by structural factors, for example the degree to which firms in a particular region concentrate on production of bulky commodities or more customeroriented niche production.     

Temperate and boreal forest tree phenology: from organ-scale processes to terrestrial ecosystem models

Key message

We demonstrate that, beyond leaf phenology, the phenological cycles of wood and fine roots present clear responses to environmental drivers in temperate and boreal trees. These drivers should be included in terrestrial ecosystem models.

Context

In temperate and boreal trees, a dormancy period prevents organ development during adverse climatic conditions. Whereas the phenology of leaves and flowers has received considerable attention, to date, little is known regarding the phenology of other tree organs such as wood, fine roots, fruits, and reserve compounds.

Aims

Here, we review both the role of environmental drivers in determining the phenology of tree organs and the models used to predict the phenology of tree organs in temperate and boreal forest trees.

Results

Temperature is a key driver of the resumption of tree activity in spring, although its specific effects vary among organs. There is no such clear dominant environmental cue involved in the cessation of tree activity in autumn and in the onset of dormancy, but temperature, photoperiod, and water stress appear as prominent factors. The phenology of a given organ is, to a certain extent, influenced by processes in distant organs.

Conclusion

Inferring past trends and predicting future trends of tree phenology in a changing climate requires specific phenological models developed for each organ to consider the phenological cycle as an ensemble in which the environmental cues that trigger each phase are also indirectly involved in the subsequent phases. Incorporating such models into terrestrial ecosystem models (TEMs) would likely improve the accuracy of their predictions. The extent to which the coordination of the phenologies of tree organs will be affected in a changing climate deserves further research.

     

Ecological factors controlling the abundance of non-native invasive black cherry (Prunus serotina) in deciduous forest understory in Belgium

The relation between invasion success of Prunus serotina and type of recipient habitat was studied in a large forest in central Belgium. The major emphasis in this study was the determination of factors controlling the abundance of P. serotina in understory strata. Environmental variables measured in 34 sample plots were slope, aspect, litter depth, soil type, pH, soil compaction, soil moisture, air humidity, soil temperature and light intensity in spring and late summer. Site conditions were also expressed indirectly for 210 sample plots using Ellenberg indicator values (soil nutrients, acidity, moisture, light conditions). Plots with P. serotina had lower mean indicator values for soil moisture, reaction (pH) and nitrogen, compared to plots without P. serotina. Twenty indicator species were identified for plots in which P. serotina occurs. The species richness of the herb layer was negatively correlated with the percentage cover of black cherry in the shrub layer. The percentage cover of P. serotina saplings in different overstory types was ranked as follows: Quercus > Pinus > Fagus > logging areas. Only three variables explained significant amounts of variation in Prunus abundance: slope, light intensity at 120 cm in April and light intensity at ground level in September. We found a positive response of black cherry seedlings to light intensity between 58 and 80% of full light (April measurements at 120 cm), while saplings showed a negative response within this range. Between 21 and 47% of full light (April measurements at 120 cm), seedlings were poorly represented whereas saplings showed a quite high cover. Between 0.3 and 1.8% light (September measurements at ground level), seedlings were almost absent while saplings maintained a high abundance. The results suggest that P. serotina shows a differential response to light intensity in relation to its development stage, i.e. the species is heliophilous at the seedling stage and becomes a shade plant at the sapling stage.     

Pulmonary disposition of erythromycin, azithromycin, and clarithromycin in foals

The objectives of the present study were to determine and compare the pulmonary disposition of azithromycin, clarithromycin, and erythromycin in foals. A single dose (10 mg/kg) of azithromycin, clarithromycin, or erythromycin was administered intragastrically to six healthy 1- to 3-month-old foals using an orthogonal design. Activity of the drugs was measured in serum, pulmonary epithelial lining fluid (PELF), and bronchoalveolar lavage (BAL) cells by use of a microbiologic assay. Peak drug activity in PELF was significantly higher in foals treated with clarithromycin (48.96+/-13.26 microg/mL) than in foals treated with azithromycin (10.00+/-7.46 microg/mL). Quantifiable erythromycin activity in PELF was only found in two of six foals. Peak drug activity in BAL cells was not significantly different between azithromycin (49.92+/-26.94 microg/mL) and clarithromycin (74.20+/-45.80 microg/mL) but activity for both drugs was significantly higher than that of erythromycin (1.02+/-1.11 microg/mL). Terminal half-life of azithromycin in serum (25.7+/-15.4 h), PELF (34.8+/-30.9 h), and BAL cells (54.4+/-17.5 h) was significantly longer than that of both clarithromycin and erythromycin. Peak azithromycin and clarithromycin activity was significantly higher in BAL cells, followed by PELF, and serum. In contrast, peak erythromycin activity in BAL cells was not significantly different from that of serum.