The Climate-Species-Matrix to select tree species for urban habitats considering climate change

Two hundred and fifty urban woody species are used in Central European parks and gardens. Based on reliable publications we attempt, for the first time, to extensively classify and assess them with regards to their usability after predicted climate changes. A new Climate-Species-Matrix has been developed for this purpose. In a two-dimensional assessment, four degrees of drought resistance and winter robustness are the decisive criteria. The woody species (divided into trees of more than 10 m in potential height and trees/shrubs of up to 10 m in height) were placed into 16 categories by decreasing tolerance, ranging from 1-1 (very suitable) to 4-4 (very limited usability). For many of these species, as well as many others that are not mentioned in this study, not all questions could be answered. Nonetheless, this categorization provides a sound basis for decisions in planning the use of woody species in cities. This planning process must also include additional criteria, dependent on individual requirements such as, soil parameters, shade resistance, aesthetics, etc. This paper is therefore meant to be a basis for discussion and supplementation for further research.     

Pesticide contamination of the upper Elbe River and an adjacent floodplain area

Journal of Soils and Sediments - Pesticide contamination of river waters is a global problem, and therefore, authorities regularly monitor the water quality status. Especially, flood events might...     

Emended descriptions of indole negative and indole positive isolates of Brachyspira (Serpulina) hyodysenteriae

Two type/reference strains of Brachyspira (B.) hyodysenteriae, 14 Belgian and German indole negative, and 14 Belgian, German and Swedish indole positive field isolates of strongly β-haemolytic intestinal spirochaetes were compared by pulsed-field gel electrophoresis (PFGE) patterns, biochemical reaction patterns, 16S rDNA sequences and MIC determinations of six antibacterial substances. Three tests for indole production, including a spot indole test, were compared with congruent results. All field isolates were classified as B. hyodysenteriae due to a high genetic and phenotypic similarity with the type strains. The Belgian and German indole negative isolates had identical and unique PFGE patterns for the tested restriction enzymes MluI and SalI, as well as identical 16S rDNA sequences, and they could not be differentiated by any of the methods used. Seven unique PFGE patterns were achieved from the 14 indole positive field isolates. The patterns were identical and unique for epidemiologically related isolates. Type/reference strains and isolates without known relation to other tested isolates showed unique banding patterns. The MICs of tylosin, tiamulin, erythromycin, clindamycin, carbadox and virginiamycin were determined in broth for all isolates. In contrast to Belgian and German isolates, the majority of the Swedish field isolates were susceptible to tylosin, erythromycin and clindamycin. Probable pathways of infection for some of the Swedish isolates were determined. The PFGE patterns of epidemic clones of B. hyodysenteriae remained stable for a period of up to 8 years. In vivo development of resistance to macrolide and lincosamide antibiotics due to use of tylosin was clearly indicated for two epidemic clones.     

Reactivity of secondary hydroxyl groups in methylβ-d-xylopyranoside toward aβ-o-4-type quinone methide

Methyl-d-xylopyranoside was allowed to react with-O-4-type quinone methide without a catalyst to elucidate the reactivities of secondary hydroxyl groups at the C2, C3, and C4 positions. Benzyl ether-type lignin-carbohydrate complex (LCC) compounds linked at the C2 and C4 positions were predominant, at a ratio of 23. However, the reactivity of the hydroxyl group at the C3 position was quite low. These results strongly suggest that the reactivity of the C2 hydroxyl group in xylan toward quinone methide intermediate is higher than that of the C3 hydroxyl group during biosynthesis of LCCs.     

Growth and mortality in underplanted tree seedlings in response to variations in canopy closure of Norway spruce stands

Six broadleaved tree species and Picea abies (L.) Karst. wereplanted under spruce plantations of varying densities, in Sweden.Treatments included control (994 stems ha^–1), dense (538stems ha^–1), sparse (294 stems ha^–1) and gap (0stems ha^–1) overstory treatments. There was an increasein height and diameter growth from control to sparse overstorytreatment of all underplanted tree species except for ash (Fraxinusexcelsior L.) and Norway maple (Acer platanoides L.). Site conditionsmay have hampered the growth of these species, as well as wildcherry (Prunus avium L.). Both oak (Quercus robur L.) and sprucehad greater growth in the gap treatment, relative to the othertreatments. Insecticide application did not influence seedlinggrowth or survival. The performance of beech (Fagus sylvaticaL.), lime (Tilia cordata Mill.), spruce and oak was consistentwith shade tolerance ranking. Beech and lime had a very highsurvival rate, even under the densest canopy. The growth andmortality of ash, maple and wild cherry differed significantlyfrom what was expected. This experiment demonstrated significantvariation in interspecific growth and mortality between sevenplanted tree species in relation to canopy density. Correctsite and species selection is crucial when underplanting inshelterwood systems.     

Identifying the biological effects of pre-commercial thinning on diameter growth in young Scots pine stands

Data from seven Scots pine (Pinus sylvestris L.) stands in central Sweden that had undergone pre-commercial thinning (PCT) were used to investigate the biological effect of PCT on the diameter at breast height (DBH) growth of the remaining trees. Two treatments were considered: a PCT treatment and a control (C) with no PCT. The DBH of the trees in each stand was measured on up to four occasions over 15 years. We examined mean DBH and DBH growth of the largest 300, 600, 900 and 1200 trees ha^?1. Two methods of selecting the trees used to calculate the mean DBH values for each measurement occasion were considered: the actual mean DBH (Dma), which is based on the DBH distribution of the trees on the measurement occasion in question, and the genuine mean DBH (Dmg), which is based on the DBH distribution of the trees on the final measurement occasion of the study and therefore focuses on the same set of trees for all measurement occasions. There was no clear difference between the Dma- and Dmg-based DBH increments, but the Dmg values tended to be somewhat larger both for the C and PCT treatments. Over a 15-year period, the relative mean yearly increments (Dma/Dmg) for different tree size classes ranged from 0.91 to 0.98, with lower values for the C treatment and larger DBH size classes. We found that PCT promotes DBH growth: over a 15-year period, the increased growth amounted to about 2.0 mm year^?1 compared to the trees in unthinned plots.     

Changes in arterial PO₂, physiological blood parameters and intracellular antioxidants in free-swimming Atlantic cod (Gadus morhua) exposed to varying levels of hyperoxia

Free-swimming Atlantic cod (Gadus morhua) were exposed to water oxygen pressures (P _wO₂) ranging from 18.1 to 41.5 kPa and sampled for blood using an indwelling caudal artery cannula. Arterial blood oxygen pressure (P _aO₂) increased with increasing P _wO₂, from 12.0 kPa in normoxia (18.1 kPa) to 34.2 kPa in the highest hyperoxic level tested (41.5 kPa). Blood CO₂ pressure and plasma bicarbonate concentration increased with P _wO₂, indicating reduced ventilation with increased P _wO₂. Plasma glucose, sodium and potassium were not affected by water oxygen level. Blood oxidative stress biomarkers, reduced glutathione, oxidized glutathione and the oxidative stress index (ratio between oxidized and total glutathione) differed intermittently between normoxia and hyperoxia. The oxidative stress index was higher in the blood of exposed compared to unexposed control cod. Together with elevated P _aO₂, these findings suggest increased production of reactive oxygen species and increased oxidative stress in Atlantic cod exposed to hyperoxia.     

Respiration and growth of a fungus, Mortierella isabellina, in response to grazing by Onychiurus armatus (Collembola)

Colonies of the fungus Mortierella isabellina (Oudem) were grazed by the collembolan Onychiurus armatus (Tullb.) for short periods interrupted by incubation without grazing in laboratory experiments. The grazed fungus had a lower respiration than ungrazed when Collembola were present on the mycelium. Fungal respiration was significantly increased with grazing when Collembola were periodically removed from the mycelium. Metal contamination of the substrate increased fungal respiration, regardless of grazing. Length of fungal mycelium was significantly greater in a natural soil in the presence of Collembola but reduced in a metal-polluted soil. Factors that may determine the impact of grazing on fungi are discussed.     

Effects of metal pollution on the earthwormdendrobaena rubida (Sav.) in acidified soils

Survival of adultDendrobaena rubida, cocoon production, cocoon viability, and growth of juveniles were examined in laboratory experiments when the worms were reared in acidified and metal polluted soils. Solutions of Cu, Cd and Pb were added to give total concentrations of 10, 100 and 500 μg g^?1 in soils with a pH of 4.5, 5.5 and 6.5. Adult tissues, hatchlings and cocoons were analyzed for metals. D. rubida survived poorly in soils with low pH, especially in combination with Pb or Cu, which accumulated in seminal vesicles and cerebral ganglion. Cocoon production was halved when pH was lowered from 6.5 to 4.5 and metals reduced the cocoon number even more in the most acid soils. Hatching success was lower than 20 % in acidified soils. In contrast, the number of hatchlings increased when pH decreased and peaked in soils polluted with Cd. While low pH reduced the embryonic development time, metals prolonged it. Juveniles grew slowly and died early at low pH.