Tolerance to acid soil conditions of the velvet beans Mucuna pruriens var. utilis and M. deeringiana

Velvet beans, fast growing leguminous cover crops used in the humid tropics, are shallow rooted on acid soils. This might be due to an inherent branching pattern, to an intrinsic toxicity of the acid subsoil or to a relative preference for root development in the topsoil. Such preference could be based on soil chemical factors in the subsoil or on physical factors such as penetration resistance or aeration. In a field experiment with two species of velvet bean (Mucuna pruriens var. utilis and M. deeringiana) all topsoil was removed and plants were sown directly into the acid subsoil. Root development was neither affected by this treatment nor by P fertilization or liming. In the absence of topsoil good root development in the exposed upper layer of subsoil was possible, so the hypothesis of a toxicity per se of the subsoil could be rejected. To test whether poor root development in the subsoil in the presence of topsoil is due to an inherent branching pattern of the plant or to a relative preference for topsoil, a modified in-growth core technique was used. Local topsoil and subsoil and an acid soil with a higher exchangeable Al content were placed in mesh bags at different depths and at different bulk densities, with and without lime and/or P fertilizer. A comparison of root development in mesh bags placed in the topsoil or subsoil showed that position and thus inherent branching pattern is not important. Root development in the subsoil was poor when this soil was placed in a mesh bag in the topsoil, but in an acid soil of much higher exchangeable Al content and higher percentage Al saturation more roots developed. In a second experiment in mesh bags, bulk density of the repacked soil in the range 1.0–1.5 g cm^-3 had no significant effect on root development. P fertilization and a high rate of liming of the soil placed in the mesh bag had a positive effect on root length density. It is concluded that poor root development in the acid subsoil under field conditions is due to a relative preference for topsoil. Al saturation and bulk density of the soil are not directly involved in this preference, but differences in availability of P and Mg or in Ca/Al ratios might play a role.     

Al avoidance and Al tolerance ofMucuna pruriens var.utilis: Effects of a heterogeneous root environment and the nitrogen form in the root environment

InMucuna pruriens var.utilis, grown with nitrate-N in a hydroponic split-root system, an Al avoidance reaction of root growth was observed, which was ascribed to local P stress in the Al containing compartment. The Al avoidance reaction was similar to the avoidance ofMucuna roots of acid subsoil in the field where roots grew preferentially in the topsoil. In the present paper the effect of different N forms (NO₃ ^– and NH₄ ⁺) on the reactions ofMucuna to Al were studied, since in acid soils N is present as a mixture of NO₃ ^– and NH₄ ⁺. No interaction between the N form and Al toxicity was found. A hydroponic split-root experiment with NH₄NO₃ nutrition, which is comparable to the situation in the field, showed that under these conditions Al avoidance did not occur. It is concluded that a relation between the Al avoidance reaction ofMucuna and P stress is still likely.Abbreviations D_r root diameter - L_pr total root length per plant - L_rw specific root length - NRA nitrate reductase activity - S/R shoot: root ratio     

The effects of lime and phosphorus on the function of wheat roots in acid top soils and subsoils

Two wheat varieties with differing aluminium tolerance were grown in pots of acid soil. Liming did not change significantly the amounts of chemically extractable P and K, but caused improved vegetative growth, increased inflow of P and K and reduced uptake of Al. Without lime, roots had a higher content and concentration of P than shoots; liming reversed this. Without lime the sensitive variety with a shorter root length had an Al inflow ten times that of the tolerant one: tolerance involves a mechanism for exlcuding Al. The inflow of P per unit inflow of Al (mol ratio) without lime was three times greater for the tolerant variety which therefore has more P to counteract the effects of Al. The same varieties were grown in two-layer soil columns, with a low P status and a limed topsoil and acid subsoil. Liming the subsoil improved plant growth but this was still restricted by low P availability. Addition of P to the topsoil caused good growth regardless of subsoil acidity: root growth increased in both layers and P (labelled with³²P) taken up from the topsoil was translocated to roots in the subsoil. This P inactivated root Al and allowed the roots to grow and take up more P from the acid subsoil with however a reduction in inflow. The sensitive variety was affected more by the acid subsoil and low P availability, had a similar ability to translocate P to subsoil roots but could not attain the growth rate of the tolerant wheat even with P and lime.     

Effects of heavy metal soil pollution and acid rain on growth and water use efficiency of a young model forest ecosystem

In a 4-year lysimeter experiment, we investigated the effects of topsoil heavy metal pollution (3,000 mg kg⁻¹ Zn, 640 mg kg⁻¹ Cu, 90 mg kg⁻¹ Pb and 10 mg kg⁻¹ Cd) and (synthetic) acid rain (pH 3.5) on tree growth and water use efficiency of young forest ecosystems consisting of Norway spruce (Picea abies), willow (Salix viminalis), poplar (Populus tremula) and birch (Betula pendula) trees and a variety of understorey plants. The treatments were applied in a Latin square factorial design (contaminated vs uncontaminated topsoil, acidified rain vs ambient rain) to 16 open-top chambers, with 4 replicates each. Each open-top chamber contained two lysimeters, one with a calcareous, and the other with acidic subsoil. The four tree species responded quite differently to heavy metal pollution and type of subsoil. The fine root mass, which was only sampled at the end of the experiment in 2003, was significantly reduced by heavy metal pollution in P. abies, P. tremula and B. pendula, but not in S. viminalis. The metal treatment responses of above-ground biomass and leaf area varied between years. In 2002, the heavy metal treatment reduced above-ground biomass and leaf area in P. tremula, but not in the other species. In 2003, metals did not reduce above-ground growth in P. tremula, but did so in the other species. It appears that the responses in above-ground biomass and leaf area, which paralleled each other, were related to changes in the relative competitive strength of the various species in the two experimental years. S. viminalis gained relative to P. tremula in absence of metal stress, in particular on calcareous subsoil, while P. abies showed the largest increases in growth rates in all treatments. Above- and below-ground growth was strongly inhibited by acidic subsoil in S. viminalis and to a lesser degree also in P. abies. In P. abies, this subsoil effect was enhanced by metal stress. Acid rain was not found to have any substantial effect. Whole-system water use efficiency was reduced by metal stress and higher on calcareous than on acidic subsoil.     

Tolerance to acid soil conditions of the velvet beans Mucuna pruriens var. utilis and M. deeringiana

Fast growing, climbing leguminous cover crops such as the velvet beans can be used to reclaim weed-infested, degraded soils in the humid tropics, especially land covered by the grass Imperata cylindrica; they climb over the grass leaves and shade the grass out if their cover lasts long enough. Tolerance of two species of velvet bean to eroded soils was investigated by removing topsoil and directly sowing into the subsoil; plots where topsoil was not removed were used as a control. The response to small amounts of P fertilizer and lime was also tested. Removal of the topsoil resulted in retarded growth of both species, in increased dry matter content of the shoot, in decreased specific leaf area and in increased leaf weight ratio, due to shorter internodes. Six weeks after planting the leaf area index (LAI) was about 1.2 where topsoil was retained, sufficient for a shading effect on Imperata. Where topsoil had been removed, the LAI was only 0.6. Mucuna pruriens var. utilis showed a faster aboveground growth than M. deeringiana; the species did not differ in tolerance to eroded soil. Small amounts of P fertilizer had no significant effect on the growth of both Mucuna species. Shoot: root ratios, on a dry weight basis, were much lower when topsoil had been removed, about 3.7 and 2.4 for M. p. utilis and M. deeringiana respectively, compared to 6.2 and 3.3 where topsoil was retained. Removal of topsoil led to reduced Mg and to increased Al concentrations in roots, and to increased levels of Mn and Al in shoots. In the second year no effect of lime or residual effect of P application was found on growth of Mucuna or Imperata. Removal of the topsoil had little effect on the growth of weeds after the cover crop had been harvested. Due to the high Al tolerance of Imperata, reclamation by Mucuna will be less effective if the topsoil has been lost by erosion.     

Characteristic responses of three tropical legumes to the inoculation of two species of VAM fungi in Andosol soils with different fertilities

The growth and mineral nutrition responses were evaluated of three tropical legumes, cowpea (Vigna unguiculata L. cv Kuromame), pigeonpea [Cajanus cajan L. (Millsp.) cv ICPL 86009] and groundnut (Arachis hypogaea cv Nakateyutaka) inoculated with two different species of VAM fungi, Glomus sp. (Glomus etunicatum-like species) and Gigaspora margarita, and grown in Andosols with different fertilities [Bray II-P: topsoil (72 ppm), subsoil (<0.1 ppm)]. Percent fungal root colonization was high in cowpea and groundnut but relatively low in pigeonpea in both soil types. Despite the low rate of root infection, significant growth responses were produced, especially in the inoculated pigeonpea plant. In all legumes, shoot dry matter production was favoured by the inoculations. Increases in shoot biomass due to mycorrhizae were greater in the subsoil than in the topsoil. Mycorrhization raised shoot concentrations of P and Ca (in cowpea and groundnut) and P and K (in pigeonpea) in the topsoil. Whereas the P concentration in shoots in the subsoil was not positively affected by VAM fungi, particularly in cowpea and pigeonpea, the concentration of K in such plants was significantly increased by VAM treatment. The results also showed that mycorrhizal enhancement of shoot micronutrient concentrations was very rare in all plants, with negative effects observed in certain cases. Cu concentration, in particular, was not affected by VAM formation in any of the plants, and Mn and Fe in pigeonpea and groundnut, respectively, remained the same whether plants were mycorrhizal or not. In both soils the three legumes responded to Glomus sp. better than to Gigaspora margarita, and the effects of the VAM fungi on each of the crops relative to the controls were greater in the subsoil than in the topsoil. However, shoot growth of groundnut was not affected as much as cowpea and pigeonpea by the type of soil used. In spite of the relatively low infection of its root, pigeonpea was generally the most responsive of the three legume species in terms of mycorrhizal/nonmycorrhizal ratios.     

Potential importance of the subsoil for the P and Mg nutrition of wheat

A method is described which allowed the quantification of the potential uptake of P and Mg from the subsoil (>30cm) by spring wheat. Wheat was grown on an artificial topsoil (sand with no plant available P or Mg) which was superimposed on loess subsoils in N. Germany. The supply of P and Mg in the topsoil was varied by application of different quantities of P and Mg fertilizer. Uptake of P and Mg from the subsoil was calculated as the difference between total plant uptake (determined by plant analysis) and the quantities of P and Mg removed from the topsoil (determined by soil analysis). P uptake from the subsoil increased from 37% to 85% of total P uptake, with decreasing P supply in the topsoil. Calculations of potential supply by diffusion showed that, with a CAL-extractable P₂O₅ content in the subsoil of 9 mg 100g^-1, supply from the subsoil was only possible if the influence of root hairs was considered. The method also showed that the total demand for Mg by spring wheat could be satisfield from the supply of Mg from the subsoil of typical loess soils. Mg uptake from the subsoil decreased to 33% of total uptake with increasing Mg supply in the topsoil.     

生活污水慢渗生态处理对土壤及杨树生长的影响

为了观测生活污水杨树林地处理对土壤和林木生长的影响,2008—2009年在郑州市龙湖镇,采用不同水力负荷(0、3、6、9、12、15cm/周),进行了污水慢渗生态处理试验。测定了污水处理期间杨树地上部分生长量,对表层(0—40cm)和下层(40—100cm)土壤理化性质进行了分析。选用土壤容重、有机质、全氮、全磷、全钾、速效氮、速效磷、速效钾作为土壤质量因子,运用土壤质量综合指标评价不同处理表层土壤质量,对下层土壤的理化性状的变化进行了研究。结果表明:在3—9cm/周水力负荷时,表层土壤质量综合指标值(QI值)和杨树地上部分生长量均随着水力负荷的增加而增加,在9cm/周水力负荷时达到最大;水力负荷大于9cm/周,QI值和杨树地上部分生长量随着水力负荷增加而降低。在水力负荷较低时,污水处理对下层土壤性状影响较小,水力负荷大于9cm/周,污水处理对下层土壤性状产生了不良影响。生活污水杨树林地处理比较适宜的水力负荷是6—9cm/周。     

双色蜡蘑对黑松幼苗生长量及其根系形态的影响

为研究双色蜡蘑(Laccaria bicolor)对黑松(Pinus thunbergii)幼苗生长及其根系形态的影响,在营养杯培育条件下,用双色蜡蘑液体菌剂对黑松幼苗进行接种处理,接种第15、30、60、90、120天时取样,比较接种和未接种黑松幼苗的生物量、根系形态及根系分形维数的差异。结果表明:双色蜡蘑在黑松幼苗地上植株、地下根系的生长及其生物量的积累方面都表现出明显的促进作用。接种双色蜡蘑也显著改善了根系总长度、分支数、表面积、体积等参数和根系分形维数,并对地下根系生长的促进作用时间早于地上部分,且效应显著高于地上部分。接种双色蜡蘑第15~30天时对地上部分基本无影响,但对根系促进作用明显,而地上部分在第60天时开始表现出显著的生长效应。研究发现,双色蜡蘑能够成功定殖于黑松根部,促进黑松幼苗生长及其生物量的积累,同时显著促进根系总长度、分支数、表面积和体积增加,并使根系分形维数增大,表现出明显的促生作用,且对根系发育的显著促进作用早于地上部分。     

Fine Root Dynamics and Forest Production Across a Calcium Gradient in Northern Hardwood and Conifer Ecosystems

Losses of soil base cations due to acid rain have been implicated in declines of red spruce and sugar maple in the northeastern USA. We studied fine root and aboveground biomass and production in five northern hardwood and three conifer stands differing in soil Ca status at Sleepers River, VT; Hubbard Brook, NH; and Cone Pond, NH. Neither aboveground biomass and production nor belowground biomass were related to soil Ca or Ca:Al ratios across this gradient. Hardwood stands had 37% higher aboveground biomass (P = 0.03) and 44% higher leaf litter production (P < 0.01) than the conifer stands, on average. Fine root biomass (<2 mm in diameter) in the upper 35 cm of the soil, including the forest floor, was very similar in hardwoods and conifers (5.92 and 5.93 Mg ha⁻¹). The turnover coefficient (TC) of fine roots smaller than 1 mm ranged from 0.62 to 1.86 y⁻¹ and increased significantly with soil exchangeable Ca (P = 0.03). As a result, calculated fine root production was clearly higher in sites with higher soil Ca (P = 0.02). Fine root production (biomass times turnover) ranged from 1.2 to 3.7 Mg ha⁻¹ y⁻¹ for hardwood stands and from 0.9 to 2.3 Mg ha⁻¹ y⁻¹ for conifer stands. The relationship we observed between soil Ca availability and root production suggests that cation depletion might lead to reduced carbon allocation to roots in these ecosystems.     

Macropore effects on phosphorus acquisition by wheat roots – a rhizotron study

Background and aims

Macropores may be preferential root pathways into the subsoil. We hypothesised that the presence of macropores promotes P-uptake from subsoil, particularly at limited water supply in surface soil. We tested this hypothesis in a rhizotron experiment with spring wheat (Triticum aestivum cv. Scirocco) under variation of fertilisation and irrigation.

Methods

Rhizotrons were filled with compacted subsoil (bulk density 1.4 g cm^?3), underneath a P-depleted topsoil. In half of these rhizotrons the subsoil contained artificial macropores. Spring wheat was grown for 41 days with and without irrigation and ³¹P–addition. Also, a ³³P–tracer was added at the soil surface to trace P-distribution in plants using liquid scintillation counting and radioactive imaging.

Results

Fertilisation and irrigation promoted biomass production and plant P-uptake. Improved growing conditions resulted in a higher proportion of subsoil roots, indicating that the topsoil root system additionally promoted subsoil nutrient acquisition. The presence of macropores did not improve plant growth but tended to increase translocation of ³³P into both above- and belowground biomass. ³³P–imaging confirmed that this plant-internal transport of topsoil-P extended into subsoil roots.

Conclusions

The lack of penetration resistance in macropores did not increase plant growth and nutrient uptake from subsoil here; however, wheat specifically re-allocated topsoil-P for subsoil root growth.

     

Water regime of metal-contaminated soil under juvenile forest vegetation

In a three-year factorial lysimeter study in Open Top Chambers (OTCs), we investigated the effect of topsoil pollution by the heavy metals Zn, Cu, and Cd on the water regime of newly established forest ecosystems. Furthermore, we studied the influence of two types of uncontaminated subsoils (acidic vs. calcareous) and two types of irrigation water acidity (ambient rainfall chemistry vs. acidified chemistry) on the response of the vegetation. Each of the eight treatment combinations was replicated four times. The contamination (2700 mg kg^–1 Zn, 385 mg kg^–1 Cu and 10 mg kg^–1 Cd) was applied by mixing filter dust from a non-ferrous metal smelter into the upper 15 cm of the soil profile, consisting of silty loam (pH 6.5). The same vegetation was established in all 32 lysimeters. The model forest ecosystem consisted of seedlings of Norway spruce (Picea abies), willow (Salix viminalis), poplar (Populus tremula) and birch (Betula pendula) trees and a variety of herbaceous understorey plants. Systematic and significant effects showed up in the second and third growing season after canopies had closed. Evapotranspiration was reduced in metal contaminated treatments, independent of the subsoil type and acidity of the irrigation water. This effect corresponded to an even stronger reduction in root growth in the metal treatments. In the first two growing seasons, evapotranspiration was higher on the calcareous than on the acidic subsoil. In the third year the difference disappeared. Acidification of the irrigation water had no significant effect on water consumption, although a tendency to enhance evapotranspiration became increasingly manifest in the second and third year. Soil water potentials indicated that the increasing water consumption over the years was fed primarily by intensified extraction of water from the topsoil in the lysimeters with acidic subsoil, whereas also lower depths became strongly exploited in the lysimeters with calcareous subsoil. These patterns agreed well with the vertical profiles of fine root density related with the two types of subsoil. Leaf transpiration measurements and biomass samples showed that different plant species in part responded quite differently and occasionally even in opposite ways to the metal treatments and subsoil conditions. They suggest that the year-to-year changes in treatment effects on water consumption and extraction patterns were related to differences in growth dynamics, as well as to shifts in competitiveness of the various species. Results showed that the uncontaminated subsoil offered a possibility to compensate the reduction in root water extraction in the topsoil under drought, as well as metal stress.     

Deepened snow cover increases grassland soil carbon stocks by incorporating carbon inputs into deep soil layers

Climate-induced changes in snow cover can greatly impact winter soil microclimate and spring water supply. These effects, in turn, can influence plant and microbial activity and the strength of leaching processes, potentially altering the distribution and storage of soil organic carbon (SOC) across different soil depths. However, few studies have examined how changes in snow cover will affect SOC stocks, and even less is known about the impact of snow cover on SOC dynamics along soil profiles. By selecting 11 snow fences along a 570 km climate gradient in Inner Mongolia, covering arid, temperate, and meadow steppes, we measured plant and microbial biomass, community composition, SOC content, and other soil parameters from topsoil to a depth of 60 cm. We found that deepened snow increased aboveground and belowground plant biomass, as well as microbial biomass. Plant and microbial carbon input were positively correlated with grassland SOC stocks. More importantly, we found that deepened snow altered SOC distribution along vertical soil profiles. The increase in SOC caused by deepened snow was much greater in the subsoil (+74.7%; 40–60 cm) than that in the topsoil (+19.0%; 0–5 cm). Additionally, the controls on SOC content under deepened snow differed between the topsoil and subsoil layers. The increase in microbial and root biomass jointly enhanced topsoil C accumulation, while the increase in leaching processes became critical in promoting subsoil C accumulation. We conclude that under deepened snow, the subsoil had a high capacity to sink C by incorporating C leached from the topsoil, suggesting that the subsoil, originally thought to be climate insensitive, could have a higher response to precipitation changes due to vertical C transport. Our study highlights the importance of considering soil depth when assessing the impacts of snow cover changes on SOC dynamics.     

Stable isotope analysis of water extraction from subsoil in upland rice (<Emphasis Type="Italic">Oryza sativa</Emphasis> L.) as affected by drought and soil compaction

Water extraction from subsoil in upland rice (Oryza sativa L.) was examined as related to topsoil desiccation and subsoil compaction. The water extraction was observed by measurements of heavy water concentrations in transpiring plants. The plants were grown in pots that were filled with sandy soil and vertically compartmented into two columns. Heavy water was applied to the subsoil. Plants exposed to mild topsoil desiccation (–120 kPa in water potential) eventually increased water extraction from the subsoil and maintained photosynthetic rate and stomatal conductance at the wet condition level. The rates of the plants subjected to severely droughted topsoil (–190 kPa) were significantly lowered due to less water uptake from the subsoil. Subsoil compaction at bulk densities of 1.45 and 1.50 Mg m^–3 inhibited increase of root length densities. Limited water extraction from the subsoil was insufficient to maintain plant productivity under drought conditions. Daily water uptake per unit of root length in the lower tube did not apparently increase even if water demand on the unit root length increased. When water to topsoil was completely withheld, water extraction from the subsoil gradually increased as the topsoil dried out. Plants that were watered and rewatered took up very little water from the subsoil. The extraction from the subsoil occurred only when water potential of the topsoil was below about –190 kPa.     

Frankia strains of soil underBetula pendula: Behaviour in soil and in pure culture

A K/Rb isotope dilution method was used to determine the uptake of K from undisturbed subsoils. Rb was applied to the topsoil (0–30 cm) to trace the K taken up from the topsoil by crops. The K/Rb ratio in the crops increases when roots contact the Rb-free subsoil. This change in the K/Rb ratio enables the calculation of the uptake of K from the subsoil. Results of 34 field experiments on loess-parabrown soils in N. Germany showed that the subsoil (>30 cm) supplied, on average, 34% of the total K uptake by spring wheat (range 9–70%). The range between the experimental sites is considered in relation to the contents of K in the top and subsoils (as extracted by 0.025 N CaCl₂ solution), the proportion of the total root length in the subsoils, and competition for K between roots in the top and subsoil. In subsoils with similar K contents, uptake from the subsoil decreased significantly from 65 to 21% of total K uptake, as K contents in the topsoils increased from 4 to 8 mg K/100 g. On sites with the same K contents in topsoils (9 mg K/100 g), the subsoil supplied 12 to 61% of total K uptake as the K contents of the subsoil increased from 2 to 27 mg K/100 g. The contribution of uptake of K from the subsoil increased with the development of the crop, from 8% at first node stage to 35% at ear emergence, as the proportion of total root length in the subsoil increased. High root length densities in the topsoil (9 cm/cm³) resulted in competition for K between roots and increased uptake of K from the subsoil.     

低磷胁迫对雷公藤幼苗形态指标及生物量的影响

采用土培的方法,研究了磷(P)胁迫对雷公藤(Tripterygium wilfordii Hook.f.)1年生和3年生幼苗在一个生长季内形态指标及生物量的影响。结果表明:低P处理显著抑制了雷公藤幼苗地上部分的增长,而对地下部分的影响较小,导致根冠比的增加,在相同P水平处理下,3年生雷公藤的根冠比高于1年生的;低P胁迫显著影响了雷公藤的生物量积累及分配,雷公藤幼苗总生物量及1年生雷公藤细根生物量占根系生物量的比例下降,根系生物量在总生物量中的比例及3年生雷公藤细根生物量在根系生物量中的比例上升。这表明3年生雷公藤对P逆境有更好的适应机制,对低P林地套种雷公藤的苗龄选择有参考价值;雷公藤幼苗的株高、最长枝均与生物量呈显著的正相关,可作为耐低P雷公藤良种选育中优良性状的指标。中轻度的P胁迫不显著影响根系生物量的积累,维持较大比例的根系是雷公藤适应低P胁迫的主要策略。     

Subsoil root activity in tree-based cropping systems

An increasing number of studies indicate that (i) nutrient and water resources can be abundant in the subsoil and (ii) trees have deep root systems that can possibly reach these resources. It is less clear whether subsoil resources are actually improving water and nutrient status of tree-based cropping systems and whether they are significantly increasing crop production and yield. To answer such a question, the distribution of nutrient and water uptake by trees needs to be quantified. So-called `root activity distributions' give valuable information about actual subsoil use by trees whereas studies on root length or mass distributions do not often correlate with uptake distributions. Despite the usually lower relative root activity in the subsoil compared to the topsoil per unit soil, the large volume of subsoil in comparison to mostly shallow topsoil is an important resource for crop nutrient and water uptake. The present study compares published root activity distributions using the model Activity=A _max(1–k ^depth). The obtained regression constants k of 0.91–0.99 determined in this publication reflect the values computed by an earlier published survey for root biomass ranging from tundra to those of temperate forest biomes. Thus, tree crops can have shallow root activity and 75% of their total root activity in the first 0.1 m of soil, or very deep root activity with more than 90% below 0.1 m. Neither environmental factors (i.e., climate and soil properties available from these publications) nor plant species explain differences of root activity distributions with depth. The deepest root activity is found for fruit trees such as citrus, guava and mango. Shaded crops such as coffee and cacao tend to have shallower root activity than fruit trees. Monocots including oil palm, coconut or banana have root activity that can be both deep and shallow. Regional and temporal variations of subsoil root activity for the same tree species are significant and generally larger than differences between species. Root activity patterns of tree crops appear to be sufficiently flexible to allow for subsoil resource use. Consequently, management such as pruning, fertilization, liming and irrigation are shown to significantly affect subsoil root activity.     

Decomposition and stabilization of root litter in top- and subsoil horizons: what is the difference?

Mechanisms leading to high mean residence times of organic matter in subsoil horizons are poorly understood. In lower parts of the soil profile root material contributes greatly to soil organic matter (SOM). The objective of this study was to elucidate the decomposition dynamics of root-derived C and N in different soil depths during a 3 year field experiment and to examine the importance of different protection mechanisms as well as abiotic factors for the decomposition dynamics. Additionally, we assessed the effect of root litter addition on native SOM. Our conceptual approach included the exposure of litterbags with ¹³C and ¹⁵N labeled wheat root material mixed to loamy agricultural soil at three different soil depths (30, 60 and 90 cm). During the incubation period, we monitored soil temperature, humidity and the incorporation of root derived C and N into the soil microbial biomass and physical SOM fractions. Our results showed that abiotic decay conditions were better in subsurface horizons compared to the topsoil. Root litter addition significantly increased the size of microbial biomass in all three soil horizons. In the topsoil, root-derived C decomposition was significantly higher in the first 6 months of incubation compared to subsoil horizons. In 60 and 90 cm depths, a lag phase with development of soil microbial biomass seemed to be prevailing before decomposition was activated. For root-derived N, similar decomposition kinetics could be observed in top- and subsoil horizons. Despite of higher SOM contents, better soil structure and higher microbial activity in the topsoil horizon compared to subsoil horizons, the amounts of root-derived C and N remaining after 3 years were similar for all three depths. Most of the root-derived C and N was present as organo-mineral complexes or occluded in soil aggregates (oPOM), illustrating similar importance of these two protection mechanisms in all three soil depths. Addition of fresh root litter caused small losses of native soil C whereas native N was retained. We conclude that despite of similar SOM protection mechanisms, there are distinct differences in decomposition dynamics of root litter between top- and subsoil horizons. In the long run, the better abiotic decay conditions prevailing in subsoil horizons may compensate for their poorer physico-chemical characteristics.     

Performance of Anisantha (Bromus) tectorum and Rumex acetosella in sandy calcareous soil

Many plants are adapted to an eroded landscape with a large proportion of virgin soil. Open and disturbed soils are today almost only restricted to agricultural fields with high loads of fertilizers. We conducted a pot experiment in order to investigate growth and nutritional constraints of one calcicole species, Anisantha (syn. Bromus) tectorum, and one calcifuge species, Rumex acetosella, in decalcified topsoil and recently exposed calcareous subsoil from a field experiment in sandy grassland. In the pot experiment we implemented one treatment where we limed topsoil with CaCO₃ to the same amount as in subsoil.The subsoil had approximately 10% CaCO₃ and both species grew less in this soil compared to the topsoil, which had less than 1% CaCO₃. Germination rate of A. tectorum was higher in subsoil than in topsoil or limed topsoil. P fertilization of the limed topsoil counteracted the negative liming effect for A. tectorum, but only partly so for R. acetosella. P fertilization of subsoil increased the shoot biomass of A. tectorum, but not of R. acetosella. P concentration in plants was not reduced when growing on subsoil or limed topsoil compared to topsoil. The results show that lime addition may reduce the P availability also to calcicole species such as A. tectorum and we found indications for that Ca toxicity may be a causing factor for the calcifuge behavior of R. acetosella. The significance of the results for conservation management practices in sandy grasslands is discussed.     

Changes in root morphology of white lupin (Lupinus albus L.) and its adaptation to soils with heterogeneous alkaline/acid profiles

The ability of Lupinus albus L. to adapt to a heterogeneous soil profile containing acid subsoil below limed topsoil of the same type, and to utilize nutrients by significantly altering its root system structure, was investigated using specially constructed soil profile tubes. Plants grown in homogeneous acid profiles had the fastest growth while those grown in homogeneous limed-soil profiles showed the slowest growth and exhibited some chlorosis after 19 days. Limed topsoil combined with an acid subsoil profile initially retarded plant growth similar to that in a homogeneous limed soil. However, after 68 days significantly greater growth had occurred in the limed/acid soil treatment relative to the homogeneous limed soil, indicating plants had benefited from the acid subsoil stratum. Plants in the homogeneous limed soil profile had lower concentrations of P, Fe and Mn in shoots compared with those in heterogeneous soils. In contrast, the concentration of Ca increased by 74%, due mainly to an increase in the water-soluble Ca fraction. When grown in a heterogeneous limed/acid soil profile, concentrations of P, Ca, K, Mg, Fe, Mn and Zn in shoots were comparable to those grown in a soil with a homogeneous acid profile. Although total root production was lower in the homogeneous limed-soil profile compared to the acid-soil containing profiles, cluster root mass was maintained at a level comparable with that in acid soil. The roots in heterogeneous soil profiles exhibited extensive plasticity, demonstrating a root-type specific, morphological response to the soil conditions. Within the acid subsoil of a heterogeneous profile, there was a large increase in cluster root mass compared with non-cluster roots. The proliferation of cluster roots in acid soil below limed topsoil may enhance the plant's ability to exploit this soil and facilitate the cultivation of L. albus on limed soil. This revised version was published online in August 2006 with corrections to the Cover Date.