ALBERT

Notes: Abstract. Wild radish plants deprived of, and continuously supplied with solution NO−3 for 7 d following 3 weeks growth at high NO−3 supply were compared in terms of changes in dry weight, leaf area, photosynthesis and the partitioning of carbon and nitrogen (NH2-N and NO−3-N) among individual organs. Initial levels of NO−3-N accounted for 25% of total plant N. Following termination of NO−3 supply, whole plant dry weight growth was not significantly reduced for 3 d, during which time plant NH2-N concentration declined by about 25% relative to NO−3-supplied plants, and endogenous NO−3-N content was reduced to nearly zero. Older leaves lost NO−3 and NH2-N, and roots and young leaves gained NH2-N in response to N stress. Relative growth rate declined due both to decreased net assimilation rate and a decrease in leaf area ratio. A rapid increase in specific leaf weight was indicative of a greater sensitivity to N stress of leaf expansion compared to carbon gain. In response to N stress, photosynthesis per unit leaf area was more severely inhibited in older leaves, whereas weight-based rates were equally inhibited among all leaf ages. Net photosynthesis was strongly correlated with leaf NH2-N concentration, and the relationship was not significantly different for leaves of NO3−-supplied compared to NO−3-deprived plants. Simulations of the time course of NO−3 depletion for plants of various NH2-N and NO−3 compositions and relative growth rates indicated that environmental conditions may influence the importance of NO−3 accumulation as a buffer against fluctuations in the N supply to demand ratio.

Notes: Based on review and original data, this synthesis investigates carbon pools and fluxes of Siberian and European forests (600 and 300 million ha, respectively). We examine the productivity of ecosystems, expressed as positive rate when the amount of carbon in the ecosystem increases, while (following micrometeorological convention) downward fluxes from the atmosphere to the vegetation (NEE = Net Ecosystem Exchange) are expressed as negative numbers. Productivity parameters are Net Primary Productivity (NPP=whole plant growth), Net Ecosystem Productivity (NEP = CO2 assimilation minus ecosystem respiration), and Net Biome Productivity (NBP = NEP minus carbon losses through disturbances bypassing respiration, e.g. by fire and logging). Based on chronosequence studies and national forestry statistics we estimate a low average NPP for boreal forests in Siberia: 123 gC m–2 y–1. This contrasts with a similar calculation for Europe which suggests a much higher average NPP of 460 gC m–2 y–1 for the forests there. Despite a smaller area, European forests have a higher total NPP than Siberia (1.2–1.6 vs. 0.6–0.9 × 1015 gC region–1 y–1). This arises as a consequence of differences in growing season length, climate and nutrition. For a chronosequence of Pinus sylvestris stands studied in central Siberia during summer, NEE was most negative in a 67-y old stand regenerating after fire (– 192 mmol m–2 d–1) which is close to NEE in a cultivated forest of Germany (– 210 mmol m–2 d–1). Considerable net ecosystem CO2-uptake was also measured in Siberia in 200- and 215-y old stands (NEE:174 and – 63 mmol m–2 d–1) while NEP of 7- and 13-y old logging areas were close to the ecosystem compensation point. Two Siberian bogs and a bog in European Russia were also significant carbon sinks (– 102 to – 104 mmol m–2 d–1). Integrated over a growing season (June to September) we measured a total growing season NEE of – 14 mol m–2 summer–1 (– 168 gC m–2 summer–1) in a 200-y Siberian pine stand and – 5 mol m–2 summer–1 (– 60 gC m–2 summer–1) in Siberian and European Russian bogs. By contrast, over the same period, a spruce forest in European Russia was a carbon source to the atmosphere of (NEE: + 7 mol m–2 summer–1 = + 84 gC m–2 summer–1). Two years after a windthrow in European Russia, with all trees being uplifted and few successional species, lost 16 mol C m–2 to the atmosphere over a 3-month in summer, compared to the cumulative NEE over a growing season in a German forest of – 15.5 mol m–2 summer–1 (– 186 gC m–2 summer–1; European flux network annual averaged – 205 gC m–2 y–1). Differences in CO2-exchange rates coincided with differences in the Bowen ratio, with logging areas partitioning most incoming radiation into sensible heat whereas bogs partitioned most into evaporation (latent heat). Effects of these different surface energy exchanges on local climate (convective storms and fires) and comparisons with the Canadian BOREAS experiment are discussed. Following a classification of disturbances and their effects on ecosystem carbon balances, fire and logging are discussed as the main processes causing carbon losses that bypass heterotrophic respiration in Siberia. Following two approaches, NBP was estimated to be only about 13–16 mmol m–2 y–1 for Siberia. It may reach 67 mmol m–2 y–1 in North America, and about 140–400 mmol m–2 y–1 in Scandinavia. We conclude that fire speeds up the carbon cycle, but that it results also in long-term carbon sequestration by charcoal formation. For at least 14 years after logging, regrowth forests remain net sources of CO2 to the atmosphere. This has important implications regarding the effects of Siberian forest management on atmospheric concentrations. For many years after logging has taken place, regrowth forests remain weaker sinks for atmospheric CO2 than are nearby old-growth forests.

Notes: Abstract  Until now, many extracellular matrix proteins, e.g. osteopontin and osteonectin, have been used to determine a cell’s osteogenic maturation. The disadvantage in evaluation of these proteins is their relative wide-ranging appearance throughout the osteogenic differentiation process. Thus, the aim of this study was to establish an immunohistochemical setup using E11, a marker that binds selectively to cells of the late osteogenic cell lineage. In addition, the histochemical expression of the bone matrix proteins osteonectin, osteopontin and fibronectin was compared to that of E11 using monoclonal antibodies. For light microscopical detection of osteogenic markers in cultured cells we developed a simple paraffin technique using a fibrin glue as embedding medium. This allows the handling of cultured cells such as a tissue sample and includes the use of stored biological specimens for further immunohistochemical experiments. We used newborn rat calvariae for whole tissue preparations and for isolation and cultivation of bone cells. In addition, we included the rat osteosarcoma cell line ROS 17/2.8 in this study. For the first time, we have localised E11 in osteocytes of rat calvaria preparations at the electron microscopical level. E11 was detected at plasma membranes of osteocytes and their processes, but not at those of osteoblasts. Accompanying experiments with cultured newborn rat calvaria cells and ROS 17/2.8 cells revealed E11 reactivity on a subset of cells. The results obtained confirm the suitability of the differentiation marker E11 as a sensitive instrument for the characterisation of bone cell culture systems.

Notes: Summary In a previous paper seasonal shifts of the temperature optimum (OP) and of the upper temperature compensation point (CP) of net photosynthesis were described for Hammada scoparia growing wild, and for Prunus armeniaca cultivated in the Negev Desert (Israel). In this paper the relationships between these shifts and the microclimatic conditions, plant-water relations, and plant development are studied. The energy budged of the thin, round photosynthesizing stems of H. scoparia growing in an open desert habitat differes from that of the broad leaves of P. armeniaca within the orchard. This explains the fact that daily maximum temperatures of the apricot increased until August and September, whereas maximum temperatures of H. scoparia reached a peak in May and June and decreased thereafter during the second half of the growing season. For H. scoparia a correspondence was found between the daily maximum tissue temperatures (and also the average temperatures of the warmest periods of the day) and the seasonal changes of the OP and CP values. This may indicate that the shifts in the temperature sensitivity of net photosynthesis of this plant are adaptations to the temperature conditions of the plant. This, however, cannot be the case for P. armeniaca, where during the second part of the growing season a period of rising leaf temperatures coincides with a period of decreasing OP and CP values. Therefore, the seasonal changes of the temperature dependence of net photosynthesis of P. armeniaca could not always be considered an adaptation to the prevailing temperature conditions of the plant. In this case, the changes in temperature sensitivity of photosynthesis could be due to developmental processes such as aging. In both lants the seasonal changes of the OP and CP values correspond to changes of the daily photoperiod and to changes of the daily average light intensity. It appears possible that this correlation indicates a causal relationship.

Notes: Summary The gas exchange of the apricot (Prunus armeniaca L.) growing in the runoff farm at Avdat (Negev, Israel) was measured during its growing period using temperature- and humidity-controlled chambers. Water potentials of the xylem were measured with a pressure bomb, and the mesophyll internal CO2 concentration was calculated from simultaneous measurements of net photosynthesis and transpiration. The daily changes in water potential Ψ had only little effect on the daily course of stomatal resistance. The early morning peak of CO2 uptake was reached when Ψ had already dropped to very low values. On dry days, Ψ and the relative water content of the leaf were improved at noon during the time of stomatal closure. On humid days, Ψ dropped to very low values (43.5 bar) at a high transpiration rate without causing stomatal closure, as much as on the dry days when stomata where more closed at less water stress. The observed changing sensitivity of the stomata to changes in air humidity during the season is related to the water status in the plant. This change is possibly caused by a long-term effect of stress in this habitat. The daily changes in stomatal diffusion resistance did not consistently correlate with changes of the CO2 concentration in the intercellular air spaces. In the morning a decreasing internal CO2 concentration was even inversely correlated to the stomatal response. In the afternoon the effect of an increasing internal CO2 concentration and the effect of external climate on stomatal response could be additive. However, at the time, when CO2 uptake reached a second peak in the afternoon the same value of diffusion resistance is reached at very different levels of internal CO2 concentration as compared to the morning. For the regulation of the diffusion resistance in apricot under the natural conditions, the effects of plant internal control mechanisms are overruled and/or modified by the external climatic factors of air humidity and temperature. The significance of the climate-controlled stomatal response for the existence and cultivation of this plant species in an arid habitat is discussed.

Notes: Summary Measurements of CO2 and water vapor exchange were performed on Prunus armeniaca L. with humidity- and temperature-controlled chambers under the climatic conditions of a desert habitat. In apricot, the stomatal response to changes in temperature and water-vapor concentration difference between leaf and air (WD) significantly determined the rates of gas exchange during the day (parts I and II). The effect of climate-controlled stomatal response on the transpiration/net photosynthesis (T/P)-ratio was analyzed and simulated using experiments conducted at constant temperature and/or humidity conditions for input parameters. The measured values of the T/P-ratio at naturally varying conditions of humidity and temperature were compared with calculated results of a model in which it was assumed, (1) that stomata and photosynthetic activity are not affected by air humidity and temperature, (2) that the stomata only respond with a constant photosynthetic activity to changes in WD, and (3) that the stomata respond to both, leaf temperature and air humidity with a constant photosynthetic activity. These simulations facilitated an analysis of the naturally observed changes in the T/P-ratio. The calculated T/P-ratios were very small if the simulation assumed that stomata only respond to WD at a constant photosynthetic activity. These low predicted values of the T/P-ratio were not obtained under natural conditions, since an increase in WD during the day was correlated with a temperature rise which tended to open stomata and change the photosynthetic activity. Humidity induced stomatal closure did appear to substantially reduce T/P-ratios. The measured T/P-ratio changed considerably during the year. The lowest T/P-ratios were obtained in the middle of the dry season at a time when stomata responded strongly to air humidity and when optimum of photosynthesis was reached at high temperatures. The daily average T/P-ratio calculated from the daily sum of P and T showed little change during the seasons. A high T/P-ratio was also observed at reduced rates of gas exchange. The T/P-ratios of apricot were compared with different species in different environments.

Notes: Abstract The study presents a data set of above-ground biomass (AGB), structure, spacing and fire regime, for 24 stands of pristine Siberian Scots pine (Pinus sylvestris) forests with lichens (n = 20) or Vaccinium/mosses (n = 4) as ground cover, along four chronosequences. The stands of the “lichen” site type (LT) were stratified into three chronosequences according to stand density and fire history. Allometric equations were established from 90 sample trees for stem, coarse branch, fine branch, twig and needle biomass. The LT stands exhibited a low but sustained biomass accumulation until a stand age of 383 years. AGB reached only 6–10 kgdw m−2 after 200 years depending on stand density and fire history compared to 20 kgdw m−2 in the “Vaccinium” type (VT) stands. Leaf area index (LAI) in the LT stands remained at 0.5–1.5 and crown cover was 30–60%, whereas LAI reached 2.5 and crown cover was 〉100% in the VT stands. Although nearest-neighbour analyses suggested the existence of density-dependent mortality, fire impact turned out to have a much stronger effect on density dynamics. Fire scar dating and calculation of mean and initial fire return intervals revealed that within the LT stands differences in structure and biomass were related to the severity of fire regimes, which in turn was related to the degree of landscape fragmentation by wetlands. Self-thinning analysis was used to define the local carrying capacity for biomass. A series of undisturbed LT stands was used to characterise the upper self-thinning boundary. Stands that had experienced a moderate fire regime were positioned well below the self-thinning boundary in a distinct fire-thinning band of reduced major axis regression slope −0.26. We discuss how this downward shift resulted from alternating phases of density reduction by fire and subsequent regrowth. We conclude that biomass in Siberian Scots pine forests is strongly influenced by fire and that climate change will affect ecosystem functions predominantly via changes in fire regimes.

Notes: Summary The photosynthesizing branches of Hammada scoparia, one of the typical dwarf shrubs of the Negev desert, undergo a seasonal change from succulent to xeromorphic anatomy. This trend is accompanied by a marked decrease of water content and of total water Ψ plant and osmotic Ψ π plant potential. Irrigated plants do not show such transitions. The daily courses of Ψ plant and Ψ π plant showed minima around noon and a tendency for maxima before sunrise. Turgor pressure Ψ p plant reached minima around noon and became negative (until ca.-10 bars). Generally, Ψ plant decreases with increasing water vapour concentration difference between plant and air (WD) in the first half of the day, and in the second half the reversal of this trend occurs. Mostly smaller increments of Ψ plant were correlated with larger increases in WD which lead to the conclusion that stomates closed enough to maintain transpiration at a constant value. Non-irrigated and irrigated plants showed different hysteresis loops of relation between Ψ plant and WD. Regulatory reduction of transpiration appears largely independently of Ψ plant which is in spring and with irrigated plants on a high level, with non-irrigated plants in summer on a low level. In summer the continous but decreasing drop of Ψ plant with increasing WD was interpreted as caused by a change in soil or root resistance. Independent of the seasonal state and of the Ψ plant level, H. scoparia regulates its water status within limited ranges of Ψ p plant changes: the irrigated plants on a higher level, the non-irrigated on a lower level of Ψ p plant . The water contents of the tissues of H. scoparia are linearily related to Ψ plant as well as Ψ p plant . Steeper slopes with non-irrigated plants in summer than with spring palnts and with irrigated plants during the whole season signify that in the latter a certain increment in turgor pressure corresponds to a large gain in water content while in the non-irrigated summer plants it varies only little for an identical change in Ψ p plant . This behaviour of non-irrigated wild plants apparently is due to the change of the elastic properties of the tissues in the assimilating branches.

Notes: Summary CO2 assimilation rate (A) and leaf conductance (g) were measured in the field on intact branches of 35-year-old Picea abies (L.) Karst. trees, in five plots each in a healthy and a declining stand. The declining site included trees with yellow needles. In order to separate atmospheric effects on gas exchange from effects of nutrient deficiency, direct effects of atmospheric pollutants were studied on green needles of different age classes in plots of trees at different stages of visible decline. The effects of nutrient deficiency on gas exchange were studied on a different group of trees showing needles of various degrees of yellowing. CO2 assimilation of green needles at the same leaf conductance fell somewhat only when needles had reached 5 years of age, the oldest age examined in this study. Leaf conductance decreased with increasing needle age, but green needles in the declining stand had leaf conductances similar to those of needles in the healthy stand. Stomata of needles with different magnesium concentrations responded to light and air humidity in all age classes. Thus, as long as needles were green, no dese effect was detectable up to 5 years of exposure to atmospheric emissions. Since all needles, green and yellow, were exposed to the same pollution levels, differences in gas exchange between green and yellow needles could not be explained simply in terms of long-term direct effects of air pollution. Needle magnesium contents were correlated with needle yellowing. Neither needle color change nor the magnesium concentration were related to g, but CO2 uptake at ambient CO2 levels declined with lower magnesium concentration and greater degrees of needle yellowing.