No abstract is provided for this article.
Summary The recent addition of trivalent metals to soil and their subsequent movement within the biosphere are of concern. For this reason, the sorption of chromium (Cr), yttrium (Y). rhodium (Rh), lanthanum (La), praseodymium (Pr) and gadolinium (Gd) in two contrasting acid soils has been determined. Except for Rh, the sorption of the other trivalent metals conformed well to the Langmuir equation with derived sorption parameters similar for all the trivalent species tested. Calculation of the buffer powers indicated that under both small (0·01 mmol kg −1 ) and large (1 mmol kg −1 ) trivalent metal soil loadings > 99·5% of the metals will be associated with the exchange phase with small quantities present in the bulk soil solution (<0·5%). It seems that the slight availability of metals within the bulk soil solution will slow the rate of trivalent metal bioremediation of contaminated sites.
Roots are the main plant organs that supply nutrients, water, hormones and physical support for the plant. Phosphorus (P) is one of the most limiting and important elements in root growth and crop production. The aims of this study were to investigate the effects of different sources of phosphorus treatments on root growth (root length, diameter and dry matter) of barley. The two glasshouse pot experiments results showed that under P deficiency, the weight of dry root significantly decreased and the total root length of whole plant significantly increased with decrease of root diameter. Our results suggested that soil fertility and root structure are widely recognized as important role of the soil community and plant growth, the root structure and root extension can directly and indirectly affected by soil fertility and specially P nutrient of the soil. Accordingly, root characteristics can determine the circumstance of plant growth and crop production.
No abstract is provided for this article.
Recovery of soil organic matter, organic matter turnover and mineral nutrient cycling is critical to the success of rehabilitation schemes following major ecosystem disturbance. We investigated successional changes in soil nutrient contents, microbial biomass and activity, C utilisation efficiency and N cycling dynamics in a chronosequence of seven ages (between 0 and 26 years old) of jarrah (Eucalyptus marginata) forest rehabilitation that had been previously mined for bauxite. Recovery was assessed by comparison of rehabilitation soils to non-mined jarrah forest references sites. Mining operations resulted in significant losses of soil total C and N, microbial biomass C and microbial quotients. Organic matter quantity recovered within the rehabilitation chronosequence soils to a level comparable to that of non-mined forest soil. Recovery of soil N was faster than soil C and recovery of microbial and soluble organic C and N fractions was faster than total soil C and N. The recovery of soil organic matter and changes to soil pH displayed distinct spatial heterogeneity due to the surface micro-topography (mounds and furrows) created by contour ripping of rehabilitation sites. Decreases in the metabolic quotient with rehabilitation age conformed to conceptual models of ecosystem energetics during succession but may have been more indicative of decreasing C availability than increased metabolic efficiency. Net ammonification and nitrification rates suggested that the low organic C environment in mound soils may favour autotrophic nitrifier populations, but the production of nitrate (NO3 −) was limited by the low gross N ammonification rates (≤1μgNg−1 d−1). Gross N transformation rates in furrow soils suggested that the capacity to immobilise N was closely coupled to the capacity to mineralise N, suggesting NO3 − accumulation in situ is unlikely. The C:N ratio of the older rehabilitation soils was significantly lower than that of the non-mined forest soils. However, variation in ammonification rates was best explained by C and N quantity rather than C:N ratios of whole soil or soluble organic matter fractions. We conclude that the rehabilitated ecosystems are developing a conservative N cycle as displayed by non-mined jarrah forests. However, further investigation into the control of nitrification dynamics, particularly in the event of further ecosystem disturbance, is warranted.
Summary Amino acids are substrates widely present in soils either in a free or a polymeric state and represent a large input of organic nitrogen into most terrestrial ecosystems. However, their behaviour in soil remains poorly understood. The aim of this study was to assess critically the impact of sorption on the mineralization of two contrastingly charged amino acids, lysine and leucine, in different‐sized, real soil aggregates. In a first experiment, we assessed the spatial variability of amino acid mineralization in aggregates of different sizes. After 1 day of incubation coefficients of variation of leucine mineralization were 33% in aggregates of 2–3 mm, 15% in aggregates of 3–5 mm and 14% in aggregates of 5–7 mm diameter. Coefficients of variation of lysine mineralization were, after 1 day of incubation, 24% in aggregates of 2–3 mm, 26% in aggregates of 3–5 mm and 24% in aggregates of 5–7 mm diameter. Compared with other substrates, this variability is small and could be due to the presence of degrading microorganisms in all aggregates. We also studied the activity of such microorganisms by following the evolution with time of 14 C‐amino acids in different compartments within aggregates 3–5 mm diameter (mineralized 14 C, microbial biomass 14 C, 14 C in soil solution and residual 14 C in soil). The microorganisms that degrade amino acids were able to assimilate substrates in soil solution immediately and used them preferentially for their growth and not solely for their energy production. For lysine, intense competition between adsorption and assimilation by microorganisms occurred from the start of the incubation period and persisted with time. Our results clearly show that sorption may retard biodegradation of amino acids in soil.
No abstract is provided for this article.
The magnitude and spatial localization of Ca2+, K+ and H+ fluxes in growing and non-growing Limnobium stoloniferum root hairs was determined using non-invasive, ion-selective vibrating microelectrodes. Both the spatial pattern and magnitude of the ionic flux was dependent on the particular ion in question. Both H+ and Ca2+ influx was localized almost exclusively to the tips of growing root hairs, suggesting that these fluxes may be involved in directing growth. Influx of K+ showed no distinct localization and uptake appeared uniform along the length of the root hair. Competitive inhibition of Ca2+ influx using a range of Mg2+ concentrations in dicated that the magnitude of the Ca2 + flux entering the root hair tip did not determine growth rate; however, the presence of Ca2+ on the external face of the membrane was implicit for root hair integrity. Aluminum proved to be a potent inhibitor of root hair growth. At an exogenous Al concentration of 20 |iM a complete blockage of Ca2 + influx into root hair tips was observed, suggesting that Al blockage of Ca2 + influx could be involved in Al toxicity. However, at a lower Al concentration (2 (iM), Ca2 + fluxes were unaffected while inhibition of growth was still ob served along with a distinct swelling of the root hair tip. The swelling at the root hair tips was identical in appear ance to that seen in the presence of microtubule inhibitors, suggesting that Al could influence a number of different sites at the plasma-membrane surface and within the cell. The possible role(s) of Ca2+ and H+ fluxes in directing tip growth are discussed.
The magnitude and spatial localization of Ca2+, K+ and H+ fluxes in growing and non-growing Limnobium stoloniferum root hairs was determined using non-invasive, ion-selective vibrating microelectrodes. Both the spatial pattern and magnitude of the ionic flux was dependent on the particular ion in question. Both H+ and Ca2+ influx was localized almost exclusively to the tips of growing root hairs, suggesting that these fluxes may be involved in directing growth. Influx of K+ showed no distinct localization and uptake appeared uniform along the length of the root hair. Competitive inhibition of Ca2+ influx using a range of Mg2+ concentrations in dicated that the magnitude of the Ca2 + flux entering the root hair tip did not determine growth rate; however, the presence of Ca2+ on the external face of the membrane was implicit for root hair integrity. Aluminum proved to be a potent inhibitor of root hair growth. At an exogenous Al concentration of 20 |iM a complete blockage of Ca2 + influx into root hair tips was observed, suggesting that Al blockage of Ca2 + influx could be involved in Al toxicity. However, at a lower Al concentration (2 (iM), Ca2 + fluxes were unaffected while inhibition of growth was still ob served along with a distinct swelling of the root hair tip. The swelling at the root hair tips was identical in appear ance to that seen in the presence of microtubule inhibitors, suggesting that Al could influence a number of different sites at the plasma-membrane surface and within the cell. The possible role(s) of Ca2+ and H+ fluxes in directing tip growth are discussed.
Rice (Oryza sativa L.) secretes far smaller amounts of metal-complexing phytosiderophores (PS) than other grasses. But there is increasing evidence that it relies on PS secretion for its zinc (Zn) uptake. After nitrogen, Zn deficiency is the most common nutrient disorder in rice, affecting up to 50% of lowland rice soils globally. We developed a mathematical model of PS secretion from roots and resulting solubilization and uptake of Zn, allowing for root growth, diurnal variation in secretion, decomposition of the PS in the soil, and the transport and interaction of the PS and Zn in the soil. A sensitivity analysis showed that with realistic parameter values for rice in submerged soil, the typically observed rates of PS secretion from rice are sufficient and necessary to explain observed rates of Zn uptake. There is little effect of diurnal variation in secretion on cumulative Zn uptake, irrespective of other model parameter values, indicating that the observed diurnal variation is not causally related to Zn uptake efficiency. Rooting density has a large effect on uptake per unit PS secretion as a result of overlap of the zones of influence of neighbouring roots. The effects of other complications in the rice rhizosphere are discussed.
Addition of the elements of 'IF' and of 'BrF' to alkenes can be effected by the in situ generation of these electrophiles from the halogen-AgF. For cyclohexene, 3,3,6,6-tetradeuterocyclohexene, methylenecyclohexane, styrene, and indene, these reactions are simple. However, for acenaphthylene, halogen–fluorine exchange and other reactions make the overall reaction quite complex. Electrophilic addition reactions for 1-fluoro-acenaphthylene are also described. The n.m.r. spectra of many of the products are given and discussed in some detail.