Impact of ectomycorrhizas on the concentration and biodegradation of simple organic acids in a forest soil

Simple organic acids seem to be important in many soil processes including nutrient uptake in the rhizosphere and long‐term pedogenic processes such as podzolization. The factors regulating the concentrations of these acids in soil, however, remain poorly understood. We have investigated one set of factors, namely the impact of ectomycorrhizal (Paxillus involutus) and non‐mycorrhizal Picea abies seedlings and humic acid on the concentration and dynamics of organic acids in soil solution. We did so over 10 months in laboratory columns containing soil from the E horizon of a sandy forest soil. Several organic acids were identified in the solution extracted from the root zone including oxalic, citric, malonic, succinic, acetic, formic and lactic acids at concentrations ranging from <0.1 to 2.3 µm . Both plants and ectomycorrhizas had significant effects on the concentration of organic acids in soil solution. In contrast, omitting P from the irrigation water appeared to have little effect on the concentrations. The microbial mineralization kinetics of oxalate conformed well to a single Michaelis–Menten equation. Further, the soil with the mycorrhizas had a significantly faster mineralization of oxalic acid over a wide concentration range than did the soil without ectomycorrhizas and without plants. We conclude that the oxalate flux through the soil with both trees and mycorrhizas is much faster than is evident from measurements of solution concentration at steady state. Humic acid had little effect on the concentrations of organic acids or dynamics in the soil solution. Oxalic acid concentrations in the soil solution were correlated with hyphal length, rate of microbial mineralization, soil respiration, and shoot to root weight ratio. We conclude that both mycorrhizas and plants have a large impact on organic acid cycling in forest soils.     

Impact of low-molecular-weight organic acids on the availability of phenanthrene and pyrene in soil

The impact of low-molecular-weight organic acids (LMWOAs) on the availability of phenanthrene and pyrene was investigated using laboratory batch assays. Experiments were conducted with two types of soil with different organic contents. The LMWOAs used were citric and oxalic acid. A mild solvent extraction procedure and a sorption-desorption experiment were used to predict the availability of phenanthrene and pyrene. Results showed that the extractable amounts of phenanthrene and pyrene in both soil types increased with increased citric or oxalic acid concentration. Citric acid addition promoted phenanthrene and pyrene extraction to a greater degree than oxalic acid. Compared with freshly spiked soils, the extractable amounts of phenanthrene and pyrene with the addition of LMWOAs decreased significantly after 60 days of cultivation. Soils with higher values of soil organic carbon content (f_oc) showed decreased phenanthrene and pyrene availability after the addition of LMWOAs. The sorption and desorption results also demonstrated the enhanced availability of PAHs with LMWOA addition. Phenanthrene sorption could be described using a linear model, regardless of the addition of LMWOAs. The simulated distribution constants (K_d) for phenanthrene sorption decreased significantly with the addition of LMWOAs. In contrast, phenanthrene desorption clearly increased with the addition of LMWOAs. These results suggest that the availabilities of phenanthrene and pyrene can be increased with the addition of suitable LMWOAs.     

Low‐molecular‐weight organic acids enhance desorption of polycyclic aromatic hydrocarbons from soil

The impact of low‐molecular‐weight organic acids (LMWOAs) on desorption of phenanthrene and pyrene as representative polycyclic aromatic hydrocarbons (PAHs) from a contaminated soil was investigated by using a laboratory batch experiment. Three LMWOAs were used in this study and were citric, oxalic and malic acids. The LMWOAs in aqueous solution promoted desorption of PAHs from soil significantly and demonstrated an increasing trend as the concentration of LMWOAs increased. When compared with desorption of phenanthrene and pyrene from soil to water, the addition of LMWOAs enhanced desorption of test PAHs by up to 285 and 299%, respectively. Among the three LMWOAs studied, citric acid demonstrated the greatest efficiency in promoting PAH desorption from soil. Solutions of LMWOA continuously promoted PAH removal from soil during the multiple cycles of desorption. Overall, the experimental results suggest that LMWOAs in aqueous solution could disrupt soil organic matter (SOM)–metal cation–mineral linkages in soils, resulting in the release of SOM from soil and simultaneous increase of dissolved organic carbon (DOC) in solution. The loss of SOM from soil and increase of DOC in solution are responsible for the enhanced PAH desorption from soil. The positive correlation between DOC in solution and desorbed PAHs from soil suggests that the loss of SOM from soil plays an important role in LMWOA‐enhanced desorption of PAHs from soil.     

The wood-decaying fungus Hygrophoropsis aurantiaca increases P availability in acid forest humus soil, while N addition hampers this effect

We evaluated the influence of the brown rot fungus Hygrophoropsis aurantiaca on P solubility in the humus layer of a podzolic forest soil. This fungus is known to exude large amounts of oxalic acid that may stimulate weathering of minerals and increase dissolution of humus, which in turn may increase P availability in the soil surrounding the fungus. Humus was inoculated using small wooden pieces colonised by the fungus. The presence of the fungus resulted in elevated concentration of PO₄⁻ in the humus solution. In a second experiment birch seedlings grown in the same humus were able to utilise the PO₄⁻ mobilised by the fungus to increase their internal P content. The factor determining this increased P uptake and the increased available P might be oxalate produced by fungus. The acid may directly dissolve P or change organic forms of P making it more susceptible to reaction with phosphatases. This fungal effect on P solubility diminished when N was added to the soil in the form of a slow release N fertilizer (methyl urea), or when a soil with a higher soil N concentration was used. We found a strong correlation between NH₄⁺ concentration and total organic carbon in the soil solution at high NH₄⁺ concentrations, suggesting the dissolution of humus as a result of the high NH₄⁺ content in the solution. This study demonstrates that the wood-decaying fungus H. aurantiaca influences nutrient turnover in forest soil, and thereby nutrient uptake by forest trees. An intensified harvest of forest products such as whole tree harvesting may decrease the active biomass of the wood decomposers and may thereby change the availability of P and the leaching of N.     

The effects of Fe deficiency on low molecular weight organic acid exudation and cadmium uptake by Solanum nigrum L.

Abstract

The influence of Fe-deficiency on the root exudation of low molecular weight organic acids (LMWOAs), pH alteration and cadmium (Cd) accumulation and translocation were investigated in morel (Solanum nigrum L.) in hydroponic culture experiments. Tartaric, citric, malic and acetic acids were monitored because these acids were abundant and often detected as root exudates. Results showed that Fe-deficient plants excreted large amounts of LMWOAs in comparison with Fe-sufficient plants across all Cd treatments (p <0.05). In both cases the concentrations of the four organic acids were tartaric > citric > malic > acetic. The results showed that the Fe-deficient plants with higher concentrations of LMWOAs accumulated more Cd (p <0.05) and induced a decrease in solution pH compared with the Fe-sufficient plants. Cadmium accumulation in the Fe-deficient and Fe-sufficient plants had significant positive correlations with the exudation of malic and acetic acids (p <0.05 and p<0.01). Cadmium accumulation in the Fe-sufficient plants had a significant (p<0.01) positive correlation with the exudation of tartaric acid, whereas there was a negative correlation (p<0.01) between Cd accumulation and the exudation of tartaric acid in the Fe-deficient plants. No significant correlation between the exudation of citric acid and Cd accumulation was obtained. Our results indicate that Fe-deficiency could induce Cd accumulation and translocation through an increase of LMWOAs exudation and pH alteration, both of which enhance Cd bioavailability.     

不同镉积累类型小麦根际土壤低分子量有机酸与镉的生物积累

采用土壤培养方法研究低镉积累小麦烟 86103和高镉积累小麦莱州 953不同生育期土壤低分子量有机酸含量与组成 ,及其与镉生物积累的关系。结果表明 ,不同镉积累类型小麦在高镉土壤中其根系镉含量差异不显著 ,但地上部镉浓度烟 86103显著低于莱州 953,而在低镉土壤中根系和地上部镉浓度烟 86 10 3均显著低于莱州 95 3。根际土壤有机酸 (柠檬酸、酒石酸、乙酸和丙酸 )含量及有机酸总量均为低镉品种烟 86103显著低于高镉品种莱州953。两个品种不同生育期有机酸含量均表现为柠檬酸 酒石酸 丙酸 乙酸 ,且各有机酸含量占有机酸总量的百分数表现稳定。小麦镉的生物积累与有机酸种类没有特异性关系 ,但与有机酸的总量有关。根际不同有机酸的水平对于土壤镉的复合或螯合溶解 ,在引起两品种地上部镉生物积累的差异方面起重要作用。     

The impact of trees, ectomycorrhiza and potassium availability on simple organic compounds and dissolved organic carbon in soil

The presence of tree roots and symbiotic mycorrhizal fungi is recognized to have a substantial impact on carbon dynamics in soils. In this study the effect of Pinus sylvestris seedlings and the ectomycorrhizal fungus Hebeloma crustuliniforme on a number of biogeochemical variables, mainly related to labile carbon pools was investigated. The impact of K limitation as a potential regulatory factor was also examined. Columns filled with E horizon ±plants and ±mycorrhizal fungi were incubated for 18.5 months. The results demonstrate that plants, as well as mycorrhizal fungi, significantly increased the concentrations of some simple organic acids, including oxalate, in soil solution. Observations for dissolved organic carbon were slightly contradictory but the cumulative amount found in drainage water was ∼20% higher in planted versus non-planted columns. Soil from planted treatments also showed more rapid mineralisation kinetics for oxalate. However carbon utilization (mineralisation vs. biomass) of oxalate and glucose by the soil microbial biomass was less influenced by plants. At harvest a component integration study of soil autotrophic and heterotrophic respiration was performed which revealed that both plant and mycorrhiza had a positive effect on the heterotrophic respiration. Potassium omission had little effect on the variables studied with the exception of the maximum mineralisation rate for oxalate, which increased when K was withdrawn. The results are discussed in the context of the dynamics of labile soil carbon pools and ecosystem C fluxes.     

Composition of organic solutes and respiration in soils derived from alkaline and non-alkaline parent materials

Parent material greatly influences pedogenesis and soil nutrient availability and consequently we hypothesized that it would significantly affect the amount of organic solutes in soil, many of which have been implicated in rhizosphere processes linked to plant nutrient uptake. Consequently, we investigated the influence of two contrasting parent materials in which calcite was present or absent (alkaline and non-alkaline soils) on the concentrations of dissolved organic carbon (DOC), low-molecular weight organic acids (LMWOA) and glucose in soil solution. Both soils were under Norway spruce. The dynamics of LMWOAs in soil were also investigated using ¹⁴C-labelled citrate and oxalate. Some of the mineral horizons of the alkaline soils showed significantly higher concentrations of DOC, phenolics, and fumarate in soil solution and also a higher basal respiration. No major differences were seen in organic solute status in the organic horizons of the two soil types. LMWOAs were present at low concentrations in soil solution (< 1 to 25 µM). Their mineralization rate significantly decreased with soil depth, however, overall neither their concentration or half-life in soil was markedly affected by parent material. The alkaline soils had significantly higher CO₂-to-soil organic C (SOC) ratios, and consequently SOC in the alkaline soils did not seem more chemically stable against mineralization. Considering possible DOC and CO₂ efflux rates it was suggested that the equal or larger SOC stocks in alkaline mineral soils were most likely linked to a higher net primary productivity. In conclusion, our study found that parent material exerted only a small effect on the concentration and dynamics of organic solutes in soil solution. This suggests that in comparison to other factors (e.g. vegetation cover, climate etc) parent material may not be a major regulator of the organic solute pool in soil.     

Characterization of root morphology and root-derived low molecular weight organic acids in two sweet potato cultivars exposed to cadmium

The mechanisms of low cadmium (Cd) accumulation in sweet potato cultivars are obscure. In this study, seedlings of a low-Cd (Nan88, N88) and a high-Cd cultivar (Xiang 16, X16) were grown in Hoagland’s solution containing Cd concentrations of 0 (control), 1 (Cd₁), and 10 µM (Cd₁₀) for 20 days. We analyzed the Cd accumulation, root morphology and low molecular weight organic acids (LMWOAs) excreted by the root tips (RTs). The total root length (RL) and specific root length (SRL) in X16 were greater than those in N88 following Cd treatments. In the Cd₁ treatment, RL and surface area for root diameter was ≤0.2 mm, and RTs in X16 were also greater than those in N88. LMWOAs excreted from the RTs initially increased and then decreased as Cd concentration increased. The RTs of N88 were more efficient at excreting organic acids than were those of X16. The low-Cd cultivar with lower RL and SRL displayed greater ability to excrete organic acids in Cd treatments, which can decrease Cd translocation from roots to shoots. Furthermore, root morphology and some LMWOAs released from the root tips played an important role in the differing rates of Cd accumulation in the two sweet potato cultivars.     

Competition for amino acids between wheat roots and rhizosphere microorganisms and the role of amino acids in plant N acquisition

The direct uptake of organic nitrogen compounds from the soil solution by plant roots has been hypothesised to constitute a significant source of N to the plant particularly in N limiting ecosystems. The experiments undertaken here were designed to test whether wheat roots could out-compete the rhizosphere microflora for a pulse addition of organic N in the form of three contrasting amino acids, namely lysine, glycine and glutamate. Amino acids were added at a concentration reflecting reported soil solution concentrations (100 μM) and the uptake into either plant biomass or respiration or microbial biomass and respiration determined over a 24 h chase period. The results showed that the plant roots could only capture on average 6% of the added amino acid with the remainder captured by the microbial biomass. We therefore present direct in vivo evidence to support earlier work which has hypothesised that organic N may be of only limited consequence in high input agricultural systems. We suggest that this is a result of the higher concentrations of NO₃⁻ in agricultural soil solutions, the slow movement of amino acids in soil relative to NO₃⁻, the rapid turnover of amino acids by soil microorganisms, and the poor competitive ability of plant roots to capture amino acids from the soil solution.     

Low molecular weight organic acids released from roots of durum wheat and flax into sterile nutrient solutions

Knowledge of the composition and quantity of organic substances released from roots of different plant species is necessary for understanding the chemical and biological processes in the rhizosphere. The present study was undertaken to quantify low molecular weight organic acids (LMWOAs) released from roots of five cultivars/lines of durum wheat (Triticum turgidum var. durum L.): Kyle, Sceptre, DT618, DT627, and DT637 and four cultivars/ lines of flax (Linum usitatissiumum L.): Somme, Flanders, AC Emerson, and YSED 2. Plants were grown in sterile nutrient solution cultures and amounts of organic acids exuded by roots were analyzed by gas chromatography. The LMWOAs varied significantly among both durum wheat and flax cultivars and oxalic, malonic, fumaric, succinic, acetic, malic, citric and tartaric acids were detected in root exudates of both species. Generally, oxalic and acetic acids were predominant in durum wheat exudates and oxalic, acetic and malic acids were predominant in flax root exudates. High oxalic acid concentrations occurred in root exudates of durum wheat cultivars DT627 and DT637, and flax cultivar YSED 2. Compared with the other durum wheat cultivars, Kyle released the lowest total amount of LMWOAs, whereas among the flax cultivars, YSED 2 had the highest total amount of acids secreted from roots. The data showed that the release of LMWOAs from roots was cultivar dependent. The results provide valuable background information for studying the role of root exudates in soil‐plant relationships.     

Quantitative analysis of soluble exudates produced by ectomycorrhizal roots as a response to ambient and elevated CO2

Despite its potential impact on soil carbon flow, few studies have attempted to quantify the effects of elevated carbon dioxide (CO₂) on production of exudates by mycorrhizal plants. In this study we quantified low molecular weight (LMW) organic compounds exuded by non-mycorrhizal (NM) and ectomycorrhizal (ECM) plants in relation to exposure to elevated CO₂. Scots pine seedlings, either colonized by one of eight different ECM fungi or non-mycorrhizal (NM), were exposed to either ambient (350 ppm) or elevated (700 ppm) concentrations of CO₂. Exudation of LMW organic acids (LMWOAs), amino acids, dissolved monosaccharides and total dissolved organic carbon (DOC) was determined and exudation rates were calculated per g root and fungal dry mass. CO₂ had a significant impact on exudation. Under elevated CO₂, exudation of total LMWOAs increased by 120-160%, amino acids by 250%, dissolved monosaccharides by 130-270% and DOC by 180-220% compared to ambient CO₂ treatment. Net CO₂ assimilation rates increased significantly by 41-47% for seedlings exposed to elevated CO₂. Exuded C calculated as a percentage of assimilated CO₂ increased by 41-88% in the elevated CO₂ treatment compared to ambient CO₂ treatment.     

低分子量有机酸作用下土壤中菲和芘的残留及形态

采用微宇宙试验方法,以菲和芘为多环芳烃(PAHs)代表物,研究了几种低分子量有机酸作用下黄棕壤中菲和芘的残留和形态。结果表明,老化60 d后土壤中菲和芘的残留含量明显减少;不施加有机酸的对照土壤中,菲和芘的残留含量为10.13和29.18 mg kg-1,去除率为87.33%和63.50%。与对照相比,供试浓度(0～64 mg kg-1)范围内,柠檬酸、草酸、酒石酸等3种低分子量有机酸作用下土壤中PAHs残留含量提高,去除率减小,表明供试条件下有机酸抑制土壤中菲和芘的降解;进一步分析发现,少量(≤4 mg kg-1)的有机酸即可对PAHs降解产生高的抑制效果。微生物降解在PAHs的去除中起重要作用,且芘比菲更抗微生物降解。供试条件下,可脱附态和有机溶剂提取态是土壤中菲和芘存在的主要形态,而结合态残留占总残留的比例很小(<8.5%)。3种有机酸均提高了土壤中可脱附态和有机溶剂提取态菲和芘的残留含量,施加有机酸使土壤中菲和芘的可脱附态含量较对照分别提高了46.67%～749.1%和1.83%～80.20%,有机溶剂提取态则提高了8.73%～375.2%和22.63%～114.3%;低分子量有机酸作用下结合态的菲和芘含量仍很小。     

有机酸对高岭石, 针铁矿和水铝英石吸附镉的影响

Effects of organic acids （oxalic, acetic, and citric） on adsorption characteristics of Cadmium （Cd） on soil clay minerals （kaolinite, goethite, and bayerite） were studied under different concentrations and different pH values. Although the types of organic acids and minerals were different, the effects of the organic acids on the adsorption of Cd on the minerals were similar, i.e., the amount of adsorbed Cd with an initial solution pH of 5.0 and initial Cd concentration of 35 mg L^-1 increased with increasing concentration of the organic acid in solution at lower concentrations, and decreased at higher concentrations. The percentage of Cd adsorbed on the minerals in the presence of the organic acids increased considerably with increasing pH of the solution. Meanwhile, different Cd adsorption in the presence of the organic acids, due to different properties on both organic acids and clay minerals, on kaolinite, goethite, or bayerite for different pHs or organic acid concentrations was found.     

低分子有机酸对土壤中重金属的解吸及影响因素

研究了柠檬酸、草酸、酒石酸和苹果酸对矿区土壤中重金属Pb、Cd、Cu和Zn的解吸行为,并探讨了介质pH值对其解吸土中重金属的影响。振荡解吸试验结果表明四种低分子有机酸对供试污染土壤中Pb、Cd、Cu和Zn都具有一定的解吸能力。由于土壤中重金属有效态含量较低,各重金属的解吸率都不高。在对Pb和Cd的解吸中,各低分子有机酸能力大小顺序为柠檬酸>酒石酸≈苹果酸>草酸;Cu的解吸顺序为柠檬酸>草酸>酒石酸≈苹果酸;Zn的解吸顺序为酒石酸>柠檬酸≈苹果酸>草酸。低分子有机酸随浓度的增加,其解吸能力提高。低分子有机酸对重金属的解吸量随pH值的降低而增加。     

Modelling the Fate of Chromated Copper Arsenate in a sandy Soil

Afforestation of former agricultural land changes soil characteristics such as pH and organic matter content, which may affect heavy metal solubility in the soil. In this study the effects of different tree species on heavy metal solubility were investigated at four 34 years old adjacent stands of beech (Fagus sylvatica L.), grand fir (Abies grandis Lindl.), Norway spruce (Picea abies (L.) Karst.) and oak (Quercus robur L.) planted on former agricultural land at four different sites in Denmark. The sites differ in soil characteristics and represent two texture classes (loamy sand and sandy loam). Soil pH and soil organic matter content was measured in the 16 stands and soil solution was isolated by centrifugation from three depths at four different occasions. Dissolved organic carbon (DOC), pH in the soil solution and the soil solution concentrations (availability) of Cd, Cu, Ni, Pb and Zn were determined. Analysis of variance showed that the tree species affects soil pH and organic matter content in the topsoil, but not in the lower horizons. Norway spruce and grand fir acidify more than beech and oak, and the highest amount of accumulated soil organic matter is in the topsoil under Norway spruce. The effects of tree species on soil solution pH and DOC resemble the effect on soil pH and organic matter content. Grand fir enhances the solubility of Cd and Zn in the topsoil with the lower solubility found under beech and oak and Norway spruce enhances the solubility of Cu, Ni and Pb in the top horizons. The lowest solubility of Ni and Pb is found under beech and oak, whereas the lowest Cu concentrations in the soil solution are found under grand fir. After 34 years of afforestation no effects of tree species on the concentrations of heavy metals in the soil solution from the C-horizons were found. The tree species effect on the concentration of Cd, Cu and Ni in the soil solution depends on the soil characteristics with the higher concentrations found in sandy loam soils, whereas no effect of site on the solution concentration was found for Pb and Zn. It was not possible to find a clear correlation between the soil solution concentrations of heavy metals, pH and DOC concentration.     

Determination of aluminium complexes of low molecular organic acids in soil solution from forest soils using ultrafiltration

Ultrafiltration (<1000 D) was evaluated as an analytical method for determination of Al bound to low molecular weight organic acids (LMWOA) in soil solutions from podzolised forest soils. The results were compared to those obtained by two chemical equilibrium models and a size exclusion chromatography method. The percentage of Al bound to LMWOAs was highest in the O horizon solutions (15–44%) and decreased in the deeper horizons. Citric acid was found to be the most important complex former. Generally the ultrafiltration method and modelling showed acceptable agreement. The method showed acceptable precision and good recovery of Al in the samples.     

Can root exudate components influence the availability of pyrene in soil?

Purpose

Little information is currently available regarding the influence of different root exudate components (RECs) on the availability of persistent organic pollutants in the soil environment. In this study, we investigated the impacts of different RECs including organic acids, amino acids, and fructose on the availability of pyrene as a representative polycyclic aromatic hydrocarbon (PAH) in soils.

Materials and methods

Citric acid, oxalic acid, malic acid, serine, alanine, and fructose were used in the experiments as representative RECs. Pyrene-spiked soils (TypicPaleudalfs) with present RECs were incubated for 30 days, and the available fraction of pyrene was determined using n-butanol extraction procedure.

Results and discussion

The amount of n-butanol-extractable pyrene in soil increased with the addition of tested RECs and increased when REC concentrations are enhanced within the range of 0–21 g kg^?1. The extractability of pyrene in soil with REC treatments and the enhancement ratio (r, %) of the extractable pyrene in soil by the addition of RECs after a 30-day incubation decreased in the following order: organic acids (oxalic acid ≥ citric acid > malic acid) > amino acid (alanine > serine) > fructose. This decrease was observed irrespective of soil sterilization, although the concentrations of extractable pyrene were lower in non-sterilized soils compared to sterilized soils. The concentrations of metal cations and dissolved organic matter (DOM) in solution increased when organic acids were added.

Conclusions

The tested RECs at concentrations of 0–21 g kg^?1 clearly enhanced the availability of pyrene in soils, and larger amounts of RECs resulted in higher pyrene availabilities in the tested soils. Microbial biodegradation diminished the amount of available pyrene irrespective of the presence of RECs. The mechanism of REC-influenced availability of pyrene in soil may be related to the metal dissolution and release of DOM from soil solids. The results of this study will be useful in assessing PAH-related risks to human health and the environment and will be instructive in food safety and remediation strategies at contaminated sites.     

AL uptake by black spruce seedlings: Persistence of organic acids in al treated rooting cultures

Experiments were conducted to monitor the pH and the persistence of simple organic acids (oxalic, citric, malic, glycolic acid) with and without Al complexation in rooting cultures (sand, peat, solution-only) under non-sterile conditions, and to characterize pertinent short-term responses of black spruce seedlings (Picea mariana [Mill.]) to subsequent changes in the rooting solutions. It was shown that the organic acids decayed within about five days unless the cultures were treated with a decay-controlling fungicide such as Captan, an antoxidant containing N-(trichloromethylthio)-4-cyclohexene-12-dicarboximide. Aluminum complexation did not increase the persistence of the organic acids except for oxalic acid. In all cases, the decay of the organic acids (or of the equivalent carboxylates) led to a simultaneous increase of solution pH which was most pronounced in the non-buffered solution cultures without Al. Captan did not affect the growth of black spruce seedlings, but was lethal to yellow birch (Betula alleghaniensis Britton) seedlings. The pH of tissuemized roots taken from the black spruce seedlings following treatments with oxalate and citrate (within and without Al) reflected the change of pH within the culture solutions.     

Effects of Low-Molecular-Weight Organic Acids on Soil Micropores and Implication for Organic Contaminant Availability

Experiments were conducted to study the effects of low-molecular-weight organic acids (LMWOAs) on micropore properties of black soil, red soil, lignin, and humin. Black soil and red soil were treated with four LMWOAs including malic, citric, succinic, and tartaric acids, whereas lignin and humin were treated with malic and citric acids. The results indicated that soil micropore distribution was changed by LMWOAs. Citric and malic acids reduced soil micropore surface area and volume significantly, but lignin micropores were not changed significantly by these two acids. Therefore, clogging may not be a main reason for the surface area and micropore volume reduction of soil organic matter. The release of metal ions from humin and soils was enhanced by LMWOAs, indicating the dissolution of soil mineral particles. Therefore, soil micropore reduction may result from the destruction of soil aggregates due to dissolution of mineral particles and extraction of metals from bridging sites.