E-waste projection using life-span and population statistics

Purpose

E-waste is the most rapidly growing problem throughout the world, which has serious future concerns over its management and recycling. This article proposes a simple approach for future e-waste projection which can be obtained by using life-span data of various electronic items along with incorporation of population statistics.

Methods

For this purpose, 7-year sales data of electronic items were collected, which is then used to generate various mathematical equations. These mathematical relations are then modified by incorporating life-span and population data.

Results and discussion

By comparing sales data with their life-span (average) and population statistics, future e-waste can be quantified both in terms of specified area under investigation and proposed estimation area. The following equation is thus proposed: E - waste In terms of quantity = m Waste projection year ? Life - span ? Initial data collection year + C × Population of estimation area Population of study area $$ \begin{array}{c}\mathrm{E}-\mathrm{waste}\;\\ {}\left(\mathrm{In}\ \mathrm{terms}\ \mathrm{of}\ \mathrm{quantity}\right)=\left[m\left\{\mathrm{Waste}\;\mathrm{projection}\;\mathrm{year}-\mathrm{Life}-\mathrm{span}\right\}-\mathrm{Initial}\ \mathrm{data}\ \mathrm{collection}\ \mathrm{year}+C\right]\times \frac{\mathrm{Population}\ \mathrm{of}\ \mathrm{estimation}\ \mathrm{area}}{\mathrm{Population}\ \mathrm{of}\ \mathrm{study}\ \mathrm{area}\ }\end{array} $$ Where m and C can be obtained from plotting year-wise sales data over Excel sheet.

Conclusions

Local as well as global projection of future e-waste can be possible with the help of final equation.     

Longitudinal variation in cadmium influx in intact first order lateral roots of sunflower (Helianthus annuus. L)

Aims

Contamination of sunflower (Helianthus annuus L.) by cadmium (Cd) is a concern for food and feed safety as this species accumulates Cd to a greater extent than other crops. We examined the relationships between root architecture and Cd²⁺ uptake by roots.

Methods

We determined and mathematically modelled the longitudinal variation of Cd²⁺ influx in first order roots of sunflower grown in hydroponics by using short-term exposure to ¹⁰⁹Cd-labelled solutions (0.8 to 500 nM). Thereafter, by taking into account the longitudinal variation of the influx, we simulated the uptake of Cd²⁺ for 24 h by cohorts of roots characterised by various architectural characteristics.

Results

Cd²⁺ influx at the root tip was on average 2.9 times that of the basal region close to the taproot. The simulations indicated that the total Cd²⁺ uptake by root cohorts mainly depends on 1/ the root diameter and the number of roots, 2/ the value of the Cd²⁺ influx at the basal region 3/ the stronger influx at the root tip.

Conclusion

Considering a higher Cd²⁺ influx at the root tip may be important to understand the relationship between root architecture and Cd²⁺ uptake by the root system.     

Continuous cultivation of Lactobacillus brevis NCL912 for production of gamma-aminobutyric acid

A continuous cultivation method for Lactobacillus brevis NCL912 to synthesize gamma-aminobutyric acid was developed in this work. Different dilution rates were evaluated for obtaining steady state in continuous cultivation. The results showed that steady state could be achieved at dilution rates from 0.08 to 0.12 h^?1. The highest gamma-aminobutyric acid productivity (5.11 g L^?1?h^?1) was obtained at dilution rate of 0.09 h^?1. The kinetic models were established for continuous gamma-aminobutyric acid production by using the Monod equation for microbial growth, and the Luedeking–Piret equation for product formation. The microbial growth and product formation can be described by equations $ \mu = {{{0.1234{C_S}}} \left/ {{\left( {0.9338+{C_S}} \right)}} \right.} $ and $ {Q_P}=6.86\,\mathrm{g}\,{{\mathrm{g}}^{-1 }}\mathrm{cell}\,{{\mathrm{h}}^{-1 }} $ , respectively. The production of gamma-aminobutyric acid by L. brevis NCL912 was non-growth-associated.     

Effects of negative air ions on oxygen uptake kinetics,recovery and performance in exercise: a randomized,double-blinded study

Limited research has suggested that acute exposure to negatively charged ions may enhance cardio-respiratory function, aerobic metabolism and recovery following exercise. To test the physiological effects of negatively charged air ions, 14 trained males (age: 32?±?7 years; \( \overset{\cdotp }{V}{\mathrm{O}}_{2 \max } \) : 57?±?7 mL min^?1 kg^?1) were exposed for 20 min to either a high-concentration of air ions (ION: 220?±?30?×?10³ ions cm^?3) or normal room conditions (PLA: 0.1?±?0.06?×?10³ ions cm^?3) in an ionization chamber in a double-blinded, randomized order, prior to performing: (1) a bout of severe-intensity cycling exercise for determining the time constant of the phase II \( \overset{\cdotp }{V}{\mathrm{O}}_2 \) response (τ) and the magnitude of the \( \overset{\cdotp }{V}{\mathrm{O}}_2 \) slow component (SC); and (2) a 30-s Wingate test that was preceded by three 30-s Wingate tests to measure plasma [adrenaline] (ADR), [nor-adrenaline] (N-ADR) and blood [lactate] (B_Lac) over 20 min during recovery in the ionization chamber. There was no difference between ION and PLA for the phase II \( \overset{\cdotp }{V}{\mathrm{O}}_2 \) τ (32?±?14 s vs. 32?±?14 s; P?=?0.7) or \( \overset{\cdotp }{V}{\mathrm{O}}_2 \) SC (404?±?214 mL vs 482?±?217 mL; P?=?0.17). No differences between ION and PLA were observed at any time-point for ADR, N-ADR and B_Lac as well as on peak and mean power output during the Wingate tests (all P?>?0.05). A high-concentration of negatively charged air ions had no effect on aerobic metabolism during severe-intensity exercise or on performance or the recovery of the adrenergic and metabolic responses after repeated-sprint exercise in trained athletes.     

High resolution imaging to assess oilseed species?? root hair responses to soil water stress

An imaging method was developed to evaluate crop species differences in root hair morphology using high resolution scanners, and to determine if the method could also detect root hair responses to soil water availability. High resolution (1890 picture elements (pixels) cm^?1) desktop scanners were buried in containers filled with soil to characterize root hair development under two water availability levels (?63 and ?188?kPa) for canola (Brassica napus L. cv Clearwater), camelina (Camelina sativa L. Crantz cv Cheyenne), flax (Linum usitatissimum L. cv CDC Bethune), and lentil (Lens culinaris Medik. cv Brewer). There was notable effect of available moisture on root hair geometry (RHG). At ?188?kPa, length from the root tip to the root hair initiation zone decreased and root hair length (RHL) became more variable near the root hair initiation zone as compared to ?63?kPa. For the response of primary axial RHL, significant main effects were present for both water availability (P?<?0.05) and species (P?<?0.0001); lateral RHL showed a significant main effect for both water availability (P?<?0.05) and species (P?<?0.01) as well. For both primary axial and lateral root hair density (RHD), there was a significant effect of species (P?<?0.0001), but no significant response to water availability. No water availability x species interaction was present in any case. Low available water reduced RHL in both primary axial and lateral roots. The change in RHL due to water availability was most evident in canola and camelina. Additionally, those with greater RHL $ \left( {\text{canola} = \text{camelina} > \text{flax} = \text{lentil}} \right) $ had lower RHD $ \left( {\text{canola} = \text{camelina} < \text{flax} < \text{lentil}} \right) $ in primary axial roots and a similar trend was found in lateral RHL. Both water and species had a significant effect on primary axial root surface area (RSA) (P?<?0.05) but no significant effect was found for lateral RSA. For primary axial RSA the longest and most dense root hair had the greatest RSA. This novel approach to in situ rhizosphere imaging allowed observation of species differences in root hair development in response to water availability and should be useful in future studies of rhizosphere interactions and crop water and nutrient management.     

Does radial oxygen loss and iron plaque formation on roots alter Cd and Pb uptake and distribution in rice plant tissues?

Background and Aims

Metal (e.g. Cd and Pb) pollution in agricultural soils and crops have aroused considerable attention in recent years. This study aimed to evaluate the effects of ROL and Fe plaque on Cd and Pb accumulation and distribution in the rice plant.

Methods

A rhizobag experiment was employed to investigate the correlations among radial oxygen loss (ROL), Fe plaque formation and uptake and distribution of Cd and Pb in 25 rice cultivars.

Results

Large differences between the cultivars were found in rates of ROL (1.55 to 6.88 mmol O₂ kg^?1 root d.w. h^?1), Fe plaque formation (Fe: 6,117–48,167 mg kg^?1; Mn: 127–1,089 mg kg^?1), heavy metals in shoot (Cd: 0.13–0.35 mg kg^?1; Pb: 4.8–8.1 mg kg^?1) and root tissues (Cd: 1.1–3.5 mg kg^?1; Pb: 45–199 mg kg^?1), and in Fe plaque (Cd: 0.54–2.6 mg kg^?1; Pb: 102–708 mg kg^?1). Rates of ROL were positively correlated with Fe plaque formation and metal deposition on root surfaces, but negatively correlated with metal transfer factors of root/plaque and distributions in shoot and root tissues.

Conclusions

ROL-induced Fe plaque promotes metal deposition on to root surfaces, leading to a limitation of Cd and Pb transfer and distribution in rice plant tissues.     

Spin-flip reactions of Zr + C2H6 researched by relativistic density functional theory

Density functional theory (DFT) with relativistic corrections of zero-order regular approximation (ZORA) has been applied to explore the reaction mechanisms of ethane dehydrogenation by Zr atom with triplet and singlet spin-states. Among the complicated minimum energy reaction path, the available states involves three transition states (TS), and four stationary states (1) to (4) and one intersystem crossing with spin-flip (marked by ?): ³ Zr + C ₂ H ₆ → ³ Zr-CH ₃ -CH ₃ ( ³ 1) → ³ TS _1/2 → ³ ZrH-CH ₂ -CH ₃ ( ³ 2) → ³ TS _2/3 ? ¹ ZrH₂-CH₂ = CH₂ ( ¹ 3) → ¹ TS _3/4 → ¹ ZrH ₃ -CH = CH ₂ ( ¹ 4). The minimum energy crossing point is determined with the help of the DFT fractional-occupation-number (FON) approach. The spin inversion leads the reaction pathway transferring from the triplet potential energy surface (PES) to the singlet’s accompanying with the activation of the second C-H bond. The overall reaction is calculated to be exothermic by about 231 kJ mol^?1. Frequency and NBO analysis are also applied to confirm with the experimental observed data.

Decomposition-rate estimation of leaf litter in karst forests in China based on a mathematical model

Aims

The objectives of the study were to analyze the relationship between decomposition rates and initial chemistry of leaf litter and to establish an optimal model to predict the decomposition rates of a large number of plant species in karst forests of China.

Methods

We determined the decomposition rate of leaf litter from 21 representative species in karst forests through a litterbag experiment. Using Akaike information criteria, we selected an optimal model among 925 regression models of decomposition rate based on initial chemistry indexes to estimate annual leaf-litter-decomposition rate for an additional 96 important species.

Results

Of the 21 representative species, Elaeocarpus decipiens and Phoebe sheareri exhibited the highest (62.85 %) and lowest (23.50 %) annual decomposition rates, respectively. In the first and second quarters, climatic conditions were not advantageous to decomposition, but 20 species reached their highest decomposition rate. Most of 117 tested species accumulated fewer nutrients and more non-easily-decomposed materials in their leaf litter than plant species in non-karst forests. The selected optimal model was: $ \mathrm{annual} \ \mathrm{decomposition} \ \mathrm{rate}=111.838-0.114\;\left( {\mathrm{total} \ \mathrm{carbon}} \right)+0.021\;\left( {\mathrm{total} \ \mathrm{nitrogen}} \right)+0.068\;\left( {\mathrm{total} \ \mathrm{potassium}} \right)-0.027\;\left( {\mathrm{lignin}} \right)-0.398\;\left( {\mathrm{tannin}} \right)-0.015\;\left( {\mathrm{starch}} \right) $ . Predicted annual leaf-litter-decomposition rates of the additional 96 tree species were 20–80 %.

Conclusions

This study enhances our understanding of leaf-litter decomposition for plant species in karst forests and provides a method for estimating annual leaf-litter-decomposition rates.     

Longitudinal variation in cadmium influx in sunflower (Helianthus annuus L.) roots as depending on the growth substrate,root age and root order

Aims

In a previous work, we observed a longitudinal decrease in Cd²⁺ influx starting from the root tip in first order lateral roots of sunflower (Helianthus annuus L.) grown in hydroponics. This variable influx was expected to impact the total Cd²⁺ uptake depending on the root system architecture and on how steep was the decrease of the influx. Here, we examined the influence of the culture substrate, of the age and order of lateral roots on the longitudinal variation of Cd²⁺ influx.

Methods

By using short-term exposures to ¹⁰⁹Cd-labelled solution (5 to 200 nM), we compared the longitudinal variations in Cd²⁺ roots influx depending on the growth substrate (hydroponics or sand), on the root age and order.

Results

In second order laterals, Cd²⁺ influx decreased from the apex to the root base, as for first order laterals. For sand cultures compared to hydroponics, the mean Cd²⁺ influx was lower and decreased more steeply with the distance from the apex. The influx also decreased with increasing root age and order, markedly in hydroponics but less for sand cultures.

Conclusion

Results suggested that for a given root surface area, the Cd²⁺ uptake by a root system should increase with increasing number of root tips and decreasing individual root length.     

Interaction-induced electric (hyper)polarizability in the dihydrogen–neon pair: basis set and electron correlation effects

We investigated the interaction (hyper)polarizability of neon–dihydrogen pairs by performing high-level ab initio calculations with atom/molecule-specific, purpose-oriented Gaussian basis sets. We obtained interaction-induced electric properties at the SCF, MP2, and CCSD levels of theory. At the CCSD level, for the T-shaped configuration, around the respective potential minimum of 6.437 a₀, the interaction-induced mean first hyperpolarizability varies for 5?<? R/a₀?<?10 as

$$ \left[{\overline{\beta}}_{\mathrm{int}}(R)\hbox{-} {\overline{\beta}}_{\mathrm{int}}\left({R}_{\mathrm{e}}\right)\right]/{e}^3{a_0}^3{E_{\mathrm{h}}}^{-2}=-0.91\left(R\hbox{-} {R}_{\mathrm{e}}\right)+0.50{\left(R\hbox{-} {R}_{\mathrm{e}}\right)}^2\hbox{--} 0.13{\left(R\hbox{-} {R}_{\mathrm{e}}\right)}^3+0.01{\left(R\hbox{-} {R}_{\mathrm{e}}\right)}^4. $$

Again, at the CCSD level, but for the L-shaped configuration around the respective potential minimum of 6.572 a₀, this property varies for 5?<? R/a₀?<?10 as

$$ \left[{\overline{\beta}}_{\mathrm{int}}(R)\hbox{-} {\overline{\beta}}_{\mathrm{int}}\left({R}_{\mathrm{e}}\right)\right]/{e}^3{a_0}^3{E_{\mathrm{h}}}^{-2}=-1.33\left(R\hbox{-} {R}_{\mathrm{e}}\right)+0.75{\left(R\hbox{-} {R}_{\mathrm{e}}\right)}^2-0.20{\left(R\hbox{-} {R}_{\mathrm{e}}\right)}^3+0.02{\left(R\hbox{-} {R}_{\mathrm{e}}\right)}^4. $$

Open image in new window

Graphical Abstract Interaction-induced mean dipole polarizability (\( \overline{a} \)) for the T-shaped configuration of H₂–Ne calculated at the SCF, MP2, and CCSD levels of theory

     

Peanut as a potential crop for bioenergy production via Cd-phytoextraction: A life-cycle pot experiment

Aims

The current study aimed to assess the potential of peanut (Arachis hypogaea L.) for bioenergy production via phytoextraction in cadmium (Cd) -contaminated soils and screen appropriate cultivars for this approach.

Methods

A life-cycle pot experiment was conducted to determine the biomass, seed yield, oil content and Cd accumulation of seven peanut cultivars under Cd concentration gradients of 0, 2, and 4 mg kg^?1.

Results

Peanut exhibits genotypic variations in Cd tolerance, seed production, oil content, and Cd accumulation. Exposure of plants to 2 and 4 mg kg^?1 Cd did not inhibit shoot biomass, seed yield, and oil content for most of the cultivars tested. There are large amounts of Cd accumulated in the shoots. Although the seed Cd concentration of peanut was relatively high, the Cd concentration in seed oils was very low (0.04-0.08 mg kg^?1). Among the cultivars, Qishan 208 showed significant Cd tolerance, high shoot biomass, high pod and seed yield, high seed oil content, considerable shoot Cd concentration, and the largest translocation factor and total Cd in shoots.

Conclusions

The cultivation of peanut in Cd-contaminated farmland was confirmed to be feasible for bioenergy production via phytoextraction, and Qishan 208 is a good candidate for this approach.     

The average local ionization energy as a tool for identifying reactive sites on defect-containing model graphene systems

In a continuing effort to further explore the use of the average local ionization energy $ \overline{\mathrm{I}}\left( \mathbf{r} \right) $ as a computational tool, we have investigated how well $ \overline{\mathrm{I}}\left( \mathbf{r} \right) $ computed on molecular surfaces serves as a predictive tool for identifying the sites of the more reactive electrons in several nonplanar defect-containing model graphene systems, each containing one or more pentagons. They include corannulene (C₂₀H₁₀), two inverse Stone-Thrower-Wales defect-containing structures C₂₆H₁₂ and C₄₂H₁₆, and a nanotube cap model C₂₂H₆, whose end is formed by three fused pentagons. Coronene (C₂₄H₁₂) has been included as a reference planar defect-free graphene model. We have optimized the structures of these systems as well as several monohydrogenated derivatives at the B3PW91/6-31G* level, and have computed their $ \overline{\mathrm{I}}\left( \mathbf{r} \right) $ on molecular surfaces corresponding to the 0.001 au, 0.003 au and 0.005 au contours of the electronic density. We find that (1) the convex sides of the interior carbons of the nonplanar models are more reactive than the concave sides, and (2) the magnitudes of the lowest $ \overline{\mathrm{I}}\left( \mathbf{r} \right) $ surface minima (the $ {{\overline{\mathrm{I}}}_{{\mathrm{S}\text{,}\min }}} $ ) correlate well with the interaction energies for hydrogenation at these sites. These $ {{\overline{\mathrm{I}}}_{{\mathrm{S}\text{,}\min }}} $ values decrease in magnitude as the nonplanarity of the site increases, consistent with earlier studies. A practical benefit of the use of $ \overline{\mathrm{I}}\left( \mathbf{r} \right) $ is that a single calculation suffices to characterize the numerous sites on a large molecular system, such as graphene and defect-containing graphene models.

Elevated CO2 improves root growth and cadmium accumulation in the hyperaccumulator Sedum alfredii

Aims

This study examined the effect of elevated CO₂ on plant growth, root morphology and Cd accumulation in S. alfredii, and assessed the possibility of using elevated CO₂ as fertilizer to enhance phytoremediation efficiency of Cd-contaminated soil by S. alfredii.

Methods

Both soil pot culture and hydroponic experiments were carried out to characterize plant biomass, root morphological parameters, and cadmium uptake in S. alfredii grown under ambient (350 μL L^?1) or elevated (800 μL L^?1) CO₂.

Results

Elevated CO₂ prompted the growth of S. alfredii, shoot and root biomass were increased by 24.6–36.7% and 35.0–52.1%, respectively, as compared with plants grown in ambient CO₂. After 10 days growth in medium containing 50 μM Cd under elevated CO₂, the development of lateral roots and root hairs were stimulated, additionally, root length, surface area, root volume and tip number were increased significantly, especially for the finest diameter roots. The total Cd uptake per pot was significantly greater under elevated CO₂ than under ambient CO₂. After 60 d growth, Cd phytoextraction efficiency was increased significantly in the elevated CO₂ treatment.

Conclusions

Results suggested that the use of elevated CO₂ may be a useful way to improve phytoremediation efficiency of Cd-contaminated soil by S. alfredii.     

Increased plant density of winter wheat can enhance nitrogen–uptake from deep soil

Background and Aims

Increased plant density improves grain yield and nitrogen (N)–use efficiency in winter wheat (Triticum aestivum L.) by increasing the root length density (RLD) in the soil and aboveground N–uptake (AGN) at maturity. However, how the root distribution and N–uptake at different soil depths is affected by plant density is largely unknown.

Methods

A 2–year field study using the winter wheat cultivar Tainong 18 was conducted by injecting ¹⁵?N–labeled urea into soil at depths of 0.2, 0.6, and 1.0 m under four plant densities of 135 m^?2, 270 m^?2,405 m^?2, and 540 m^?2.

Results

We observed significant RLD and ¹⁵?N–uptake increases at each soil depth as the plant density increased from 135 to 405 m^?2. ¹⁵?N–uptake increased with plant density as the soil depth increased, although the corresponding RLD value fell with depth. The ¹⁵?N–uptake at each soil depth was positively related to the RLD at the same depth. The total AGN was positively related to RLD in deep soil, especially at 0.8–1.2 m.

Conclusions

Increasing the plant density from 135 m^?2 to the optimum increases AGN primarily by increasing the RLD in deep soil and therefore increasing the plant density of winter wheat can be used to efficiently recover N leached to deep soil. Moreover, the total root numbers per unit area and RLD still increased at supraoptimal density while shoot number and N uptake stagnated.     

Phenotypic seedling responses of a metal-tolerant mutant line of sunflower growing on a Cu-contaminated soil series: potential uses for biomonitoring of Cu exposure and phytoremediation

Background and aims

The potential use of a metal-tolerant sunflower mutant line for both biomonitoring and phytoremediating a Cu-contaminated soil series was investigated.

Methods

The soil series (21–1,170 mg Cu kg^?1) was sampled in field plots at control and wood preservation sites. Sunflowers were cultivated 1 month in potted soils under controlled conditions.

Results

pH and dissolved organic matter influenced Cu concentration in the soil pore water. Leaf chlorophyll content and root growth decreased as Cu exposure rose. Their EC₁₀ values corresponded to 104 and 118 μg Cu L^?1 in the soil pore water, 138 and 155 mg Cu kg^?1 for total soil Cu, and 16–18 mg Cu kg^?1 DW shoot. Biomass of plant organs as well as leaf area, length and asymmetry were well correlated with Cu exposure, contrary to the maximum stem height and leaf water content.

Conclusions

Physiological parameters were more sensitive to soil Cu exposure than the morphological ones. Bioconcentration and translocation factors and distribution of mineral masses for Cu highlighted this mutant as a secondary Cu accumulator. Free Cu²⁺ concentration in soil pore water best predicted Cu phytoavailability. The usefulness of this sunflower mutant line for biomonitoring and Cu phytoextraction was discussed.     

Dynamic permeability of the lacunar–canalicular system in human cortical bone

A new method for the experimental determination of the permeability of a small sample of a fluid-saturated hierarchically structured porous material is described and applied to the determination of the lacunar–canalicular permeability \((K_\mathrm{LC})\) in bone. The interest in the permeability of the lacunar–canalicular pore system (LCS) is due to the fact that the LCS is considered to be the site of bone mechanotransduction due to the loading-driven fluid flow over cellular structures. The permeability of this space has been estimated to be anywhere from \(10^{-17}\;\) to \(10^{-25}\; \hbox {m}^{2}\) . However, the vascular pore system and LCS are intertwined, rendering the permeability of the much smaller-dimensioned LCS challenging to measure. In this study, we report a combined experimental and analytical approach that allowed the accurate determination of the \(K_\mathrm{LC}\) to be on the order of \(10^{-22}\; \hbox {m}^{2}\) for human osteonal bone. It was found that the \(K_\mathrm{LC}\) has a linear dependence on loading frequency, decreasing at a rate of \(2 \times 10^{-24}\; \hbox {m}^{2}\) /Hz from 1 to 100 Hz, and using the proposed model, the porosity alone was able to explain 86 % of the \(K_\mathrm{LC}\) variability.     

Growth, carboxylate exudates and nutrient dynamics in three herbaceous perennial plant species under low, moderate and high phosphorus supply

Background and aims

Australian herbaceous native species have evolved in phosphorus (P) impoverished soils. Our objective was to explore shoot and root adaptations of two of these species with potential to be developed as pasture plants, at low, moderate and high P supply after 4 and 7?weeks of growth.

Methods

A glasshouse experiment examined the effect of 5, 20 and 80?mg?P?kg^?1 air-dry soil on growth, rhizosphere carboxylate content, and mineral nutrition of two Australian native perennials, Kennedia nigricans (Fabaceae) and Ptilotus polystachyus (Amaranthaceae), and the exotic Medicago sativa (Fabaceae).

Key results

Leaf P concentrations at P80 were 6, 14 and 52?mg?P?g^?1 leaf dry weight for M. sativa, K. nigricans and P. polystachyus, respectively. As soil P concentration increased, rhizosphere carboxylate content decreased for M. sativa, increased and then decreased for K. nigricans and was unchanged for P. polystachyus. For all species, the contribution of malic acid declined at the second harvest. For all species and P treatments, the amount of rhizosphere carboxylates per unit root length decreased as root length of a plant increased. Plant P content was determined more by P uptake rate per unit root length and time than by root length. Uptake of Mo for all species, and uptake of K, Mg and Mn for P. polystachyus, increased with soil P concentration. Uptake of Fe and S was higher when the content of carboxylates in the rhizosphere was higher.

Conclusion

Root physiological adaptations (i.e. rhizosphere carboxylate content and P-uptake rate) are more important than morphological adaptations (i.e. root length and diameter) to enhance the uptake of P and cations.