Trace elements influenced by environmental changes in Lake Biwa: (I) Seasonal variations under suboxic hypolimnion conditions during 2007 and 2009

Dissolved oxygen (DO) in the Lake Biwa hypolimnion reached its lowest level of <1 mg kg^?1 in 2007. In this paper, we report the variations in the total dissolvable (TD), dissolved (D), and labile particulate (LP) fractions of Al, Si, P, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Mo, W, and U in Lake Biwa 2007 and 2009. Al and Fe species were predominantly in the form of LP-Al and LP-Fe and were strongly correlated with one another (r = 0.99), suggesting that the weathering of aluminous minerals and the supply of clay mineral particles are the main factors that influence the distributions of Al and Fe. Although D-Al increased in the summer epilimnion, D-Fe was relatively low, probably as a result of uptake by plants. Reductive release of Fe from the bottom was not seen. Mn was also dominated by LP-Mn, but this fraction showed a different distribution to those of LP-Al and LP-Fe. The D-Mn and LP-Mn concentrations varied by factors of 700–1000 and showed marked increases in the bottom water during stratification in 2007. We believe that Mn²⁺ was released from the sediments and oxidized by DO in the bottom water. Ni, Cu, Zn, and Cr, which exist as cationic species, had LP/TD ratios of 0.1–0.7 and relatively uniform distributions. Si, P, V, As, Mo, W, and U, which form oxoacid species, had LP/TD ratios of 0–0.8. Si, P, and As were characterized by nutrient-like profiles, V, W, and U showed summer maxima in the epilimnion, and Mo had a uniform distribution. TD-Mo increased in the bottom water along with TD-Mn, while TD-V and TD-W showed significant decreases. These results are likely attributable to differences in the adsorption of these elements onto manganese oxides and iron hydroxides.     

Accumulative phases for heavy metals in limnic sediments

Data from mechanical concentrates of recent sediments indicate that clay minerals, clay-rich aggregates and heavy minerals are the major carriers of heavy metals in detrital sediment fractions. Hydrous Fe/Mn oxides and carbonates and sulfides, in their specific environments, are the predominant accumulative phases for heavy metals in autochthonous fractions. Sequential chemical extraction techniques permit the estimation of characteristic heavy metal bonding forms: exchangeable metal cations, easily reducible, moderately reducible, organic and residual metal fractions, whereby both diagenetic processes and the potential availability of toxic compounds can be studied. The data from lakes affected by acid precipitation indicate that zinc, cobalt and nickel are mainly released from the easily reducible sediment fractions and cadmium from organic phases. In contrast at pH 4.4, neither lead nor copper seem to be remobilized to any significant extent. Immobilization by carbonate precipitation seems to provide an effective mechanism for the reduction of dissolved inputs 9f metals such as zinc and cadmium in pH-buffered, hard water systems.     

中亚热带不同母质发育森林土壤磷组分特征及其影响因素

本研究以福建三明砂岩和花岗岩发育的米槠林土壤和杉木林土壤为对象,分析土壤磷组分、铁铝氧化物、微生物生物量以及磷酸酶活性等指标,研究母质和森林类型对土壤磷组分的影响程度和机制。结果表明: 母质和森林类型显著影响土壤不同磷组分含量。总体上,砂岩发育土壤全磷含量、活性无机/有机磷、中等活性无机/有机磷以及惰性磷含量均显著高于花岗岩发育土壤,并且砂岩发育米槠林土壤活性有机磷含量、中等活性无机/有机磷以及惰性磷含量显著高于砂岩发育杉木林土壤,而花岗岩发育米槠林与杉木林土壤磷组分的含量差异不显著。花岗岩发育的2种森林土壤酸性磷酸酶(ACP)活性显著高于砂岩,而砂岩发育米槠林土壤微生物生物量碳(MBC)和微生物生物量磷(MBP)显著高于砂岩发育杉木林土壤。土壤不同磷组分的含量与土壤不同形态铁铝氧化物含量、MBP、MBC呈显著正相关,而与土壤pH、ACP呈显著负相关,表明土壤母质和森林类型可能主要通过土壤铁铝氧化物赋存形态、ACP、MBP等生物及非生物因子影响中亚热带森林土壤磷组分分配特征。     

Sedimentary phosphorus fractions and bioavailability as influenced by repeated sediment resuspension

Concentrations of phosphorus (P) fractions and changes in their bioavailability in the sediments as influenced by repeated resuspension were determined by sequential fractionation in laboratory experiments. The water and sediment samples used were taken from the campus canal. Sequential fractionation indicated that the concentrations of the iron bound P (BD–P) were predominant, consisting of over 50% of total P (Tot-P) in the sediments that did and did not undergo resuspension. BD–P mobility was reduced due to resuspension resulting from the decline of the proportion ratio of non-occluded Fe–P and occluded Fe–P from 0.53 to 0.29. Therefore, under sediment resuspension conditions, using the sum of loosely sorbed P (NH₄Cl–P), BD–P, aluminium bound P (Al–P), and organic-P (NaOH–nrP) to estimate bio-available P (BAP) might be problematic. However, BAP could be accurately estimated by the sum of NH₄Cl–P, % BD–P (bio-available, non-occluded Fe–P), and NaOH–nrP. By this estimation, the amount of BAP in the sediments as influenced by repeated resuspension decreased by about 10% of Tot-P, compared with the initial state (raw sediments). The results suggest that repeated resuspension could accelerate the transformation of P from mobile fractions to refractory fractions, which can be attributed to the increase of occluded Fe–P, Al–P, and calcium bound P (HCl–P).     

Aluminium in tea: SEC-ICP-MS speciation studies of infusions and simulated gastrointestinal digests

Abstract

The speciation of aluminium in tea infusions and in vitro gastrointestinal digests of tea infusions has been investigated using size exclusion chromatography coupled to inductively coupled plasma mass spectrometry (SEC-ICP-MS). At pH 2.5, following simulated gastric treatment, Al from tea eluted at a similar retention volume to that obtained for an aqueous Al standard. At pH 5.5, an aqueous Al standard was eluted from an SEC column in Tris buffer (Al recovery ≈ 100%) only in the presence of a complexing agent (NaF), and at a retention volume corresponding to a molecular mass greater than that expected for an ionic species. Aluminium associated with a tea infusion eluted in two fractions: a higher molecular weight fraction corresponding to Al strongly bound to ligands in the tea, and a lower molecular weight fraction probably comprised of labile Al eluting as Al-F complexes. Simulated gastrointestinal digestion produced three Al-bearing fractions, of which the two at higher molecular mass represented ligand-bound Al. The molarity of the Tris buffer strongly influenced the retention volume of the Al fractions, particularly for the ligand-bound Al. After simulated gastrointestinal digestion, the soluble labile fraction (15% of the Al from the tea infusion) was considered to be potentially available for absorption. The actual proportion of the fraction that might be absorbed would depend upon a number of physiological and nutritional factors.     

Phosphorus pools and internal loading in a eutrophic lake with gradients in sediment geochemistry created by land use in the watershed

Spatial variations in phosphorus (P) fractionation, sediment geochemistry, and sorptive properties for P are assessed to test the hypothesis that these sediment properties vary within the lake and are governed by different land uses in the watershed. The dynamic equilibrium between P in sediment and water is investigated using sorption–desorption isotherms. Sediments in the littoral zone were rich in iron (Fe), aluminium (Al), and clay material in comparison to sediments from the lake proper and thus had better abilities to sorb and retain P. In the limnetic zone, there was an increasing abundance of primary minerals, and the fraction of apatite-P was high, while the level of total P was low. The amount of labile adsorbed P (LAP) in the littoral sediments varied because of contrasting land use in the sub-catchments draining into different parts of the lake. Sediments in areas where forest streams enter the lake contained significantly more LAP than sediments in areas impacted by agricultural influenced streams. Internal P loading from sediments predominantly originating from forest streams is mainly governed by sediment resuspension. The dominant P pool in sediments near the inlets of agriculturally influenced streams was non-apatite inorganic P, of which the Fe-bound is a potentially important source of P under anoxic conditions.     

Four decades of post-agricultural forest development have caused major redistributions of soil phosphorus fractions

Fertilisation of agricultural land causes an accumulation of nutrients in the top soil layer, among which phosphorus (P) is particularly persistent. Changing land use from farmland to forest affects soil properties, but changes in P pools have rarely been studied despite their importance to forest ecosystem development. Here, we describe the redistributions of the P pools in a four-decadal chronosequence of post-agricultural common oak (Quercus robur L.) forests in Belgium and Denmark. The aim was to assess whether forest age causes a repartitioning of P throughout the various soil P pools (labile P, slowly cycling P and occluded P); in particular, we addressed the time-related alterations in the inorganic versus organic P fractions. In less than 40 years of oak forest development, significant redistributions have occurred between different P fractions. While both the labile and the slowly cycling inorganic P fractions significantly decreased with forest age, the organic fractions significantly increased. The labile P pool (inorganic + organic), which is considered to be the pool of P most likely to contribute to plant-available P, significantly decreased with forest age (from >20 to <10% of total P), except in the 0-5 cm of topsoil, where labile P remained persistently high. The shift from inorganic to organic P and the shifts between the different inorganic P fractions are driven by biological processes and also by physicochemical changes related to forest development. It is concluded that the organic labile P fraction, which is readily mineralisable, should be taken into account when studying the bioavailable P pool in forest ecosystems.     

Controls of Bedrock Geochemistry on Soil and Plant Nutrients in Southeastern Utah

The cold deserts of the Colorado Plateau contain numerous geologically and geochemically distinct sedimentary bedrock types. In the area near Canyonlands National Park in Southeastern Utah, geochemical variation in geologic substrates is related to the depositional environment with higher concentrations of Fe, Al, P, K, and Mg in sediments deposited in alluvial or marine environments and lower concentrations in bedrock derived from eolian sand dunes. Availability of soil nutrients to vegetation is also controlled by the formation of secondary minerals, particularly for P and Ca availability, which, in some geologic settings, appears closely related to variation of CaCO₃ and Ca-phosphates in soils. However, the results of this study also indicate that P content is related to bedrock and soil Fe and Al content suggesting that the deposition history of the bedrock and the presence of P-bearing Fe and Al minerals, is important to contemporary P cycling in this region. The relation between bedrock type and exchangeable Mg and K is less clear-cut, despite large variation in bedrock concentrations of these elements. We examined soil nutrient concentrations and foliar nutrient concentration of grasses, shrubs, conifers, and forbs in four geochemically distinct field sites. All four of the functional plant groups had similar proportional responses to variation in soil nutrient availability despite large absolute differences in foliar nutrient concentrations and stoichiometry across species. Foliar P concentration (normalized to N) in particular showed relatively small variation across different geochemical settings despite large variation in soil P availability in these study sites. The limited foliar variation in bedrock-derived nutrients suggests that the dominant plant species in this dryland setting have a remarkably strong capacity to maintain foliar chemistry ratios despite large underlying differences in soil nutrient availability.     

Phosphorus Fractions and Fluxes in the Water Column and Sediments of a Tropical Reservoir (Lobo‐Broa – SP)

Sedimentation rates of organic and inorganic matter, chlorophyll a, P fractions, Ca, Mn, Fe and Al, were determined by sediment traps in a tropical oligo‐mesotrophic reservoir of São Paulo (Brazil). Vertical profiles of the sediments were analyzed for organic content, metals, P and surface P fraction composition. Estimated mean sedimentation rates, corrected for resuspension were: total solids, 1068 g m^—2 y^—1 (OM = 44.7%); chlorophyll a, 2.1 g m^—2 y^—1 and total phosphorus, 2.9 g m^—2 y^—1. The predominant P fraction in the settling flux was associated with aluminum minerals while surface sediments were dominated by organic P. The reservoir exhibited low sediment retention of P (13.0%), Al (9.9%), Fe (9.9%), Mn (1.4%) and Ca (traces), compared to trap sedimentation. This feature was related with a high vertical dynamics (resuspension and bottom release) and with the low retention time of the system.     

Vertical distribution of biological and geochemical phosphorus subcycles in two southern Appalachian forest soils

We measured Al, Fe, and P fractions by horizon in two southern Appalachian forest soil profiles, and compared solution PO₄ ^–1 removal in chloroform-sterilized and non-sterilized soils, to determine whether biological and geochemical P subcycles were vertically stratified in these soils. Because organic matter can inhibit Al and Fe oxide crystallization, we hypothesized that concentrations of non-crystalline (oxalate-extractable) Al (Al₀) and Fe (Fe₀), and concomitantly P sorption, would be greatest in near-surface mineral (A) horizons of these soils.Al₀ and Fe₀ reached maximum concentrations in forest floor and near-surface mineral horizons, declined significantly with depth in the mineral soil, and were highly correlated with P sorption capacity. Small pools of readily acid-soluble (AF-extractable) and readily-desorbable P suggested that PO₄ ^3– was tightly bound to Al and Fe hydroxide surfaces. P sorption in CHCl₃-sterilized mineral soils did not differ significantly from P sorption in non-sterilized soils, but CHCl₃ sterilization reduced P sorption 40–80% in the forest floor. CHCl₃ labile (microbial) P also reached maximum concentrations in forest floor and near-surface mineral horizons, comprising 31–35% of forest floor organic P. Combined with previous estimates of plant root distributions, data suggest that biological and geochemical P subcycles are not distinctly vertically stratified in these soils. Plant roots, soil microorganisms, and P sorbing minerals all reach maximum relative concentrations in near-surface mineral horizons, where they are likely to compete strongly for PO₄ ^3– available in solution.     

Wheat, canola and grain legume access to soil phosphorus fractions differs in soils with contrasting phosphorus dynamics

Despite the high phosphorus (P) mobilizing capacity of many legumes, recent studies have found that, at least in calcareous soils, wheat is also able to access insoluble P fractions through yet unknown mechanism(s). We hypothesized that insoluble P fractions may be more available to non-legume plants in alkaline soils due to increased dissolution of the dominant calcium(Ca)-P pool into depleted labile P pools, whereas non-legumes may have limited access to insoluble P fractions in iron(Fe)- and aluminium(Al)-P dominated acid soils. Four crop species (faba bean, chickpea, wheat and canola) were grown on two acid and one alkaline soil under glasshouse conditions to examine rhizosphere processes and soil P fractions accessed. While all species generally depleted the H₂O-soluble inorganic P (water Pi) pool in all soils, there was no net depletion of the labile NaHCO₃-extractable inorganic P fraction (NaHCO₃ Pi) by any species in any soil. The NaOH-extractable P fraction (NaOH Pi) in the alkaline soil was the only non-labile Pi fraction depleted by all crops (particularly canola), possibly due to increases in rhizosphere pH. Chickpea mobilized the insoluble HCl Pi and residual P fractions; however, rhizosphere pH and carboxylate exudation could not fully explain all of the observed Pi depletion in each soil. All organic P fractions appeared highly recalcitrant, with the exception of some depletion of the NaHCO₃ Po fraction by faba bean in the acid soils. Chickpea and faba bean did not show a higher capacity than wheat or canola to mobilize insoluble P pools across all soil types, and the availability of various P fractions to legume and non-legume crops differed in soils with contrasting P dynamics.     

Solid-Phase Chemical Fractionation of Selected Trace Metals in Some Northern Kentucky Soils

The fractionation and distribution with depth of Cd, Cr, Cu, Ni, Pb, and Zn in 26 soils of Northern Kentucky were determined through a sequential extraction procedure in response to environmental concerns about increasing anthropogenic inputs in a fast-paced, urbanizing area. The selected sites have not received any biosolid- or industrial-waste applications. Average total concentrations per metal in soil profiles derived from alluvial, glacial till, and residual materials ranged from 0.43 to 56.00 mg kg^?1 in the sequence Zn > Ni > Pb > Cr > Cu > Cd, suggesting relatively small anthropogenic inputs. The distribution of Cu, Cr, Ni, and Zn increased with soil depth, whereas Cd and Pb remained stable, indicating a strong geological or pedogenic influence. Residual forms were most important for the retention of Cu, Zn, and Ni. Cadmium and Pb exhibited a strong affinity for the Fe-Mn oxide fraction, while Cr showed the strongest association with the organic fraction. In terms of metal mobility and toxicity potential inferred from metal concentrations in labile fractions, Cd posed the greatest risk, followed by Cr ～ Pb > Ni > Zn > Cu. Soil pH, OM, and clay content were the most important parameters explaining the partitioning of metals in labile and residual fractions, emphasizing the importance of metal fractionation in soil management decisions. Alluvial soils generally contained the highest total and labile metal concentrations, suggesting potential metal enrichment through anthropogenic additions and depositional processes. These environments exhibit the highest risk for metal mobilization due to drastic changes in redox conditions, which can destabilize existing metal retention pools.     

Importance of clay size minerals for Fe(III) respiration in a petroleum-contaminated aquifer

The availability of Fe(III)‐bearing minerals for dissimilatory Fe(III) reduction was evaluated in sediments from a petroleum‐contaminated sandy aquifer near Bemidji, Minnesota (USA). First, the sediments from a contaminated area of the aquifer, in which Fe(III) reduction was the predominant terminal electron accepting process, were compared with sediments from a nearby, uncontaminated site. Data from 0.5 m HCl extraction of different size fractions of the sediments revealed that the clay size fraction contributed a significant portion of the ‘bio‐available’ Fe(III) in the background sediment and was the most depleted in ‘bio‐available’ Fe(III) in the iron‐reducing sediment. Analytical transmission electron microscopy (TEM) revealed the disappearance of thermodynamically unstable Fe(III) and Mn(IV) hydroxides (ferrihydrite and Fe vernadite), as well as a decrease in the abundance of goethite and lepidocrocite in the clay size fraction from the contaminated sediment. TEM observations and X‐ray diffraction examination did not provide strong evidence of Fe(III)‐reduction‐related changes within another potential source of ‘bio‐available’ Fe(III) in the clay size fraction – ferruginous phyllosilicates. However, further testing in the laboratory with sediments from the methanogenic portion of the aquifer that were depleted in microbially reducible Fe(III) revealed the potential for microbial reduction of Fe(III) associated with phyllosilicates. Addition of a clay size fraction from the uncontaminated sediment, as well as Fe(III)‐coated kaolin and ferruginous nontronite SWa‐1, as sources of poorly crystalline Fe(III) hydroxides and structural iron of phyllosilicates respectively, lowered steady‐state hydrogen concentrations consistent with a stimulation of Fe(III) reduction in laboratory incubations of methanogenic sediments. There was no change in hydrogen concentration when non‐ferruginous clays or no minerals were added. This demonstrated that Fe(III)‐bearing clay size minerals were essential for microbial Fe(III) reduction and suggested that both potential sources of ‘bio‐available’ Fe(III) in the clay size fraction, poorly crystalline Fe(III) hydroxides and structural Fe(III) of phyllosilicates, were important sources of electron acceptor for indigenous iron‐reducing microorganisms in this aquifer.     

Iron content of sediment and phosphate adsorption properties

Phosphorus can occur in sediments in different forms and accordingly its availability varies. The distinction between the phosphorus fractions is made with two chemical extraction methods; an ammonium oxalate-oxalic acid extraction and an extraction according to Hieltjes & Lijklema (1980).The iron and aluminum liberated with the ammonium oxalate-oxalic acid extraction method is linearly correlated (r ² = 0.73) with the phosphorus liberated in the first two steps of the Hieltjes and Lijklema extraction by: P = 0.035 (Fe + Al) + 0.001 (P, Fe and Al in mmol g^–1).The iron and aluminum (hydr)oxides are very important fractions in the sediment adsorption capacity for phosphorus. The phosphorus sorption capacity (PSC) is 0.080 mol P (mol (Fe + Al))^–1 and the adsorption constant (k) is 11.9 µmol P l^–1. Here it is assumed that iron and aluminum (hydr)oxide have the same affinity for phosphorus.     

Soil-nutrient availability and the nutrient-use efficiencies of forests along an altitudinal gradient on Yakushima Island,Japan

The vegetation on Yakushima Island, Japan, grows on soils derived from Akahoya volcanic ash, released from the Kikai Caldera about 7300 years ago. The eruption was devastating and it is believed that primary succession and soil formation reinitiated across all altitudes at this point. We hypothesize that the concentrations of soil total phosphorus (P) and labile P fractions increase with increasing altitude because the soil formation has progressed less in upslope areas as a result of the cooler temperature and because of the ample P source of the volcanic ash. Conversely, we hypothesize that the concentration of soil inorganic nitrogen (N) decreases with increasing altitude. Available soil P and N would result in increasing P limitation downslope and increasing N limitation upslope, respectively. We studied soil P fractions and soil inorganic N, and P- and N-use efficiencies of the seven forests on Yakushima along an elevation gradient (170–1550 m a.s.l.). Contrary to our hypotheses, soil total P, labile soil P fractions, and inorganic N decreased with increasing altitude. The P- and N-use efficiencies of the forests were negatively correlated with the concentration of soil total active P (total P minus occluded P) and inorganic N, respectively. We suggest that progressive soil acidity and slower decomposition under cooler and wetter environments upslope must have dissolved the P contained in volcanic ash and accelerated P leaching. Forest ecosystems on Yakushima that show a distinct altitudinal zonation are, therefore, characterized by increasing P and N shortage with increasing altitude.     

Association with pedogenic iron and aluminum: effects on soil organic carbon storage and stability in four temperate forest soils

Soil organic carbon (SOC) can be stabilized via association with iron (Fe) and aluminum (Al) minerals. Fe and Al can be strong predictors of SOC storage and turnover in soils with relatively high extractable metals content and moderately acidic to circumneutral pH. Here we test whether pedogenic Fe and Al influence SOC content and turnover in soils with low Fe and Al content and acidic pH. In soils from four sites spanning three soil orders, we quantified the amount of Fe and Al in operationally-defined poorly crystalline and organically-complexed phases using selective chemical dissolution applied to the soil fraction containing mineral-associated carbon. We evaluated the correlations of Fe and Al concentrations, mean annual precipitation (MAP), mean annual temperature (MAT), and pH with SOC content and ¹⁴C-based turnover times. We found that poorly crystalline Fe and Al content predicted SOC turnover times (p < 0.0001) consistent with findings of previous studies, while organically-complexed Fe and Al content was a better predictor of SOC concentration (p < 0.0001). Greater site-level MAP (p < 0.0001) and colder site-level MAT (p < 0.0001) were correlated with longer SOC turnover times but were not correlated with SOC content. Our results suggest that poorly crystalline Fe and Al effectively slow the turnover of SOC in these acidic soils, even when their combined content in the soil is less than 2% by mass. However, in the strongly acidic Spodosol, organo-metal complexes tended to be less stable resulting in a more actively cycling mineral-associated SOC pool.     

Aluminium effects on Scenedesmus obtusiusculus with different phosphorus status. I. Mineral uptake

Synchronously growing cultures of the unicellular green alga Scenedesmus obtusiusculus were cultivated for 24 and 72 h in the presence or absence of phosphorus. Aluminium chloride (37, 74, 111, 148, 185, or 222 μmol) was added daily to 1 l cell suspension at the end of the cell division phase. As AlCl₃ decreases the pH of the growth medium, controls were run in media with low pH in the absence of AlCl₃. Samples for analysis of the internal (net uptake) and external (bound to cell surface) levels of Al, Mg, P, Ca, and Fe were taken every second hour during a 24 h period or once after 72 h. The investigation shows that the intracellular aluminium in Scenedesmus affects the nutrient status of the cells. A high intracellular level of Al is in consort with an enhancement of the intracellular fractions of Mg, P, Ca and Fe. The increase in net uptake of the minerals measured in the presence of Al is not due to an Al-induced lowering of the pH, caused by Al. The concentrations of Al, Mg, P, Ca and Fe in the cells are generally lower during the dark period of the cell cycle, when the cells are dividing, than during the light period. A peak in mineral concentration of the cells could be monitored in the middle of the 24 h life cycle of the cells. The intracellular Al level is higher when the growth medium is low in P than in phosphorus-rich medium, due to precipitation of aluminium-phosphate both in medium and at cell surfaces. The extracellular Al and P fractions are thus higher in the presence than in the absence of P. The highest Al content monitored in the cells is about 100 nmol Al (10⁶ cells)^?1. A large fraction of Al initially taken up after addition to the medium is subsequently released from the cells during the 24 h cell cycle. The results are interpreted as Al effects on the plasma membrane, thus indirectly affecting various mechanisms for ion transport across the membrane. There are also indications that a surface covered with aluminium-phosphate, formed at high P level in the medium, may prevent ion uptake.     

海拔梯度变化对武夷山黄山松林土壤磷组分和有效性的影响

土壤磷（P）是植物生长必需的养分元素,也是亚热带森林生产力的主要限制元素。目前,关于不同海拔土壤P组分和P有效性的变化规律尚无统一定论,其原因主要是忽略了植被类型变化导致的P组分和P有效性对海拔的响应更为复杂。因此,以武夷山不同海拔黄山松林为研究对象,通过测定土壤环境因素、理化性质、微生物生物量（SMB）、酸性磷酸单酯酶（ACP）和磷酸双酯酶（PD）活性以及土壤P组分,探究土壤P组分和P有效性的变化及其影响因素。结果表明,随海拔降低,速效P含量显著增加,而易分解P、中等易分解P、难利用P和总磷含量显著减少。冗余分析结果表明,微生物生物量磷和微生物生物量氮是影响土壤P组分和P有效性变化的关键因素。研究表明,随海拔降低,黄山松林土壤微生物通过提高ACP、PD活性和降低SMB含量的能量分配策略,促进更多较难分解P组分的矿化,从而提高速效P含量,以满足微生物对P的需求。因此,在低海拔地区,微生物通过能量分配策略获取更多有效P,可能有利于提高武夷山黄山松林土壤速效P的供应,但从长期来看,可能使P矿化速率提高和P损耗增加,导致P库的储备不足,不利于土壤P素养分的可持续供应。     

Phosphorus status of some ethiopian soils

The capacity to sorb P varied among some Ethiopian soils. Volcanic ash soils sorbed the maximum P while Fluvisols and Regosols sorbed the least. Sorption of P was significantly correlated with exchangeable and extractable forms of Fe and Al as well as pH and organic matter. But is was not related to the clay content of the soils. The role of Al was more important than that of Fe even though more dithionite and oxalate extractable Fe than Al was found in all soils.     

缙云山4种林分土壤无机磷与活性铝的含量及分布

为探索不同林分对土壤中无机磷与活性铝的含量及分布的影响,以及无机磷与活性铝之间的相互关系,以在我国西南地区酸性土壤上的农林经营管理提供理论和实践依据。研究以缙云山广泛分布的4种林分类型：山莓、马尾松、楠竹和柑橘林土壤为对象,采用酸性土壤无机磷分级方法和铝试剂比色法测定了土壤剖面A、B和C层中各形态的无机磷与活性铝的含量,分析了不同林分土壤中无机磷和活性铝的含量和分布特征。结果表明,林分类型显著影响土壤中无机磷与活性铝的含量与分布,且铁磷(Fe-P)、交换态铝(Ex-Al)和羟基铝(Hy-Al)的含量和比例还受到土壤层次的影响。4种林分相比,山莓林能促进闭蓄态磷(O-P)的形成,而马尾松、楠竹和柑橘林则有利于Al-P、Fe-P和Ca-P的形成;柑橘林有利于低活性的腐殖酸铝(Al-AH)形成,而山莓、马尾松和楠竹林促进高活性的Ex-Al或Hy-Al溶出;Ex-Al、Al-P和Fe-P在土层的分布上有表层富集现象,而Hy-Al集中分布于B层。此外,土壤Ex-Al和Al-P与Fe-P之间,Hy-Al和Ca-P之间均呈显著(P<0.05)正相关。因此,林分类型显著影响土壤无机磷与活性铝的含...