Persistence of tree related patterns in soil nutrients following slash-and-burn disturbance in the tropics

Individual trees are known to influence soil chemical properties, creating spatial patterns that vary with distance from the stem. The influence of trees on soil chemical properties is commonly viewed as the agronomic basis for low-input agroforestry and shifting cultivation practices, and as an important source of spatial heterogeneity in forest soils. Few studies, however, have examined the persistence of the effects of trees on soil after the pathways responsible for the effects are removed. Here, we present evidence from a Mexican dry forest indicating that stem-related patterns of soil nutrients do persist following slash-and-burn removal of trees and two years of cropping. Pre-disturbance concentrations of resin extractable phosphorus (P), bicarbonate extractable P, NaOH extractable P, total P, total nitrogen (N) and carbon (C), KCl extractable nitrate (NO₃ ^-), and net N mineralization and nitrification rates were higher in stem than dripline soils under two canopy dominant species of large-stemmed trees with contrasting morphologies and phenologies (Caesalpinia eriostachys Benth. and Forchhammeria pallida Liebm.). These stem effects persisted through slash burning and a first growing season for labile inorganic and organic P, NaOH inorganic P, and plant-available P, and through a second growing season for labile organic P, NaOH organic P, and plant-available P. While stem effects for extractable NO₃ ^-, net nitrification rates, total N and C disappeared after felling and slash burning, these stem effects returned after the first growing season. These results support the view that tree-influenced patterns of soil nutrients do persist after tree death, and that trees contribute to the long-term spatial heterogeneity of forest soils. This revised version was published online in June 2006 with corrections to the Cover Date.     

Organic phosphorus in soil water under a European beech (Fagus sylvatica L.) stand in northeastern Bavaria, Germany: seasonal variability and changes with soil depth

Organically bound phosphorus (P) is a mobile form of phosphorus in many soils and thus its dynamics relevant for the leaching and cycling of this element. Despite its importance, little is known about the chemical composition of dissolved organic P. We studied the concentrations, fluxes, and chemical composition of organic P in forest floor leachates and soil solutions in a Rendzic Leptosol under a 90-year-old European beech (Fagus sylvatica L.) forest over a 27-month period (1997–1999). The chemical composition of organic P was analysed using XAD-8 fractionation and ³¹P-nuclear magnetic resonance (NMR) spectroscopy. Organic P was the dominant P form in forest floor leachates as well as in porewaters of the mineral soil. The largest concentrations of organic P were observed during summer and peaked (330–400 g dissolved organic P l^–1) after rain storms following short dry periods, concurrently with the concentrations of organic carbon (OC). Because of high rainfall, fluxes of organic P (and C) were greatest in autumn although concentrations of organic C and P were lower than in summer. In forest floor leachates, the hydrophilic fraction of dissolved organic matter contained 83 ± 13% of the bulk organic P. In soil solutions from 90 cm depth, organic P was almost exclusively in the hydrophilic fraction. Because of the low retention of the hydrophilic fraction of dissolved organic matter in the mineral soils, concentrations of organic P in soil water remained almost constant with depth. Consequently, organic P contributed > 95% of the total P leached into deeper subsoils. The overall retention of organic P in the weakly developed mineral soils was little and so the average annual fluxes of organic P in subsoils at 90 cm depth (38 mg m^–2) comprised 67% of those from the forest floors (57 mg m^–2) during the study period. Hence, organic P proved to be mobile in the studied soil. ³¹P-NMR spectroscopy confirmed the dominance of organic P species in soil water. Signals due to inorganic P occurred only in spectra of samples collected in winter and spring months. Spectra of samples from summer and autumn revealed traces of condensed phosphates. Due to low P contents, identification of organic P species in samples from winter and spring was not always possible. In summer and autumn, monoester and diester phosphates were the dominant organic species and varied little in their relative distributions. The distribution of organic species changed little from forest floor leachates to the subsoil solutions indicating that the composition of P-containing compounds was not influenced by sorptive interactions or biological transformation.     

Evaluation of the phosphorus status of P-deficient podzols in temperate pine stands: combining isotopic dilution and extraction methods

Phosphorus (P) is often a limiting factor of forest growth but our knowledge of the processes governing P availability in forest soils is rather limited. In the present work, we combined a isotopic dilution method with extraction methods to evaluate the P status in Pinus pinaster plantation forests on highly P-deficient soils. Total, organic, and inorganic P, dissolved and diffusive P, i.e. ionic P species that can be transferred from the solid phase to the soil solution due a gradient of concentration, were determined to a soil depth of 120 cm in a gradient of 18 forest sites (seven humid sites, five mesic sites, and six dry sites). Our objective was to assess the potential contribution of organic and inorganic P to plant available P. Based on results and our original assumptions, we observed that the contribution of organic P fractions (mineralization of soil organic P) to P availability related to the contribution of inorganic P fractions (diffusive P for durations up to 1 year) was predominant in litter, less important in top soil horizons, and negligible at depths below 30 cm. This was partly due to a decreasing proportion of organic P and an increasing proportion of diffusive P with soil depth. Owing to a very low amount of diffusive P in the top soils in dry sites, the relative contribution of organic P was actually higher in these sites than in humid and mesic sites, despite a lower overall organic P fraction. The combination of extraction and isotopic dilution methods in our study shed new light on P status in this forest range. In particular, these methods enable assessment of both the size of the pools and their dynamic fractions.     

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...     

Nutrient fluxes in a snow-dominated, semi-arid forest: Spatial and temporal patterns

We tested five hypotheses regarding the potential effects of precipitation change on spatial and temporal patterns of water flux, ion flux, and ion concentration in a semiarid, snowmelt-dominated forest in Little Valley, Nevada. Variations in data collected from 1995 to 1999 were used to examine the potential effects of snowpack amount and duration on ion concentrations and fluxes. Soil solution NO₃ ^–, NH₄ ⁺, and ortho-phosphate concentrations and fluxes were uniformly low, and the variations in concentration bore no relationship to snowmelt water flux inputs of these ions. Weathering and cation exchange largely controlled the concentrations and fluxes of base cations from soils in these systems; however, soil solution base cation concentrations were affected by cation concentrations during snowmelt episodes. Soil solution Cl^– and SO₄ ^2– concentrations closely followed the patterns in snowmelt water, suggesting minimal buffering of either ion by soils. In contrast to other studies, the highest concentration and the majority of ion flux from the snowpack in Little Valley occurred in the later phases of snowmelt. Possible reasons for this include sublimation of the snowpack and dry deposition of organic matter during the later stages of snowmelt. Our comparison of interannual and spatial patterns revealed that variation in ion concentration rather than water flux is the most important driver of variation in ion flux. Thus, it is not safe to assume that changes in total precipitation amount will cause concomitant changes in ion inputs to this system.     

Soil Phosphorus Fractionation during Forest Development on Landslide Scars in the Luquillo Mountains,Puerto Rico1

Mineral soils from a chronosequence of landslide scars ranging in age from 1 to more than 55 years in a subtropical montane rain forest of eastern Puerto Rico were used to determine the rate at which labile P capital recovers during primary succession. Nine organic and inorganic soil P fractions were measured using the Hedley sequential extraction procedure. Deep soil cores (9 m) from a nearby site were also analyzed to determine the distribution of P fractions below the solum. Litterfall P was measured for two years in the landslide scars to estimate allochthonous litter P inputs, and published precipitation data were used to estimate annual atmospheric inputs of P to the recovering forests. In the upper solum (0–10 cm), organic matter increased with landslide age, as did resin‐Pi, labile P (defined here as resin‐Pi + HCO₃‐Pi + HCO₃‐Po) and total organic P. Occluded P decreased with increasing landslide age. No significant changes in P concentrations or pools were observed in 10 to 35 or in 35 to 60 cm depth intervals across the chronosequence. Labile soil P increased to approximately two‐thirds of the pre‐disturbance levels in the oldest landslide scar (>55 yr). Thus, plants, their associated microflora/fauna, and P inputs from off‐site substantially altered the distribution of soil P fractions during forest recovery. Across the chronosequence, the increase in labile P accumulated in soil and biomass appeared to be greater than the estimated allochthonous inputs from litter and precipitation, indicating that as the forest developed, some occluded P may have been released for use by soil biota. Resin‐Pi and labile P were correlated with soil organic matter content, suggesting, as in other highly weathered soils, organic matter accumulation and turnover are important in maintaining labile P pools. Primary mineral P (apatite) was scarce, even in deep soil cores.     

Net nitrogen mineralization and net nitrification rates in soils following deforestation for pasture across the southwestern Brazilian Amazon Basin landscape

Previous studies of the effect of tropical forest conversion to cattle pasture on soil N dynamics showed that rates of net N mineralization and net nitrification were lower in pastures compared with the original forest. In this study, we sought to determine the generality of these patterns by examining soil inorganic N concentrations, net mineralization and nitrification rates in 6 forests and 11 pastures 3 years old or older on ultisols and oxisols that encompassed a wide variety of soil textures and spanned a 700-km geographical range in the southwestern Brazilian Amazon Basin state of Rondônia. We sampled each site during October-November and April-May. Forest soils had higher extractable NO₃ ^?-N and total inorganic N concentrations than pasture soils, but substantial NO₃ ^?-N occurred in both forest and pasture soils. Rates of net N mineralization and net nitrification were higher in forest soils. Greater concentrations of soil organic matter in finer textured soils were associated with greater rates of net N mineralization and net nitrification, but this relationship was true only under native forest vegetation; rates were uniformly low in pastures, regardless of soil type or texture. Net N mineralization and net nitrification rates per unit of total soil organic matter showed no pattern across the different forest sites, suggesting that controls of net N mineralization may be broadly similar across a wide range of soil types. Similar reductions in rates of net N transformations in pastures 3 years old or older across a range of textures on these soils suggest that changes to soil N cycling caused by deforestation for pasture may be Basin-wide in extent. Lower net N mineralization and net nitrification rates in established pastures suggest that annual N losses from largely deforested landscapes may be lower than losses from the original forest. Total ecosystem N losses since deforestation are likely to depend on the balance between lower N loss rates from established pastures and the magnitude and duration of N losses that occur in the years immediately following forest clearing.     

Leaching of dissolved organic carbon,dissolved organic nitrogen,and other solutes from coarse woody debris and litter in a mixed forest in New York State

Coarse woody debris (CWD) may play a role in nutrient cycling in temperate forests through the leaching of solutes, including dissolved organic carbon (DOC) and dissolved organic nitrogen (DON), to the underlying soil. These fluxes need to be considered in element budget calculations, and have the potential to influence microbial activity, soil development, and other processes in the underlying soil, but studies on leaching from CWD are rare. In this study, we collected throughfall, litter leachate, and CWD leachate in situ at a young mixed lowland forest in NY State, USA over one year. We measured the concentrations of DOC, DON, NH₄⁺, NO₃⁻, dissolved organic sulfur, SO₄²⁻, Cl⁻, Al, Ca, K, Mg, Na, and P, estimated the flux of these solutes in throughfall, and measured the cover of CWD to gain some insight into possible fluxes from CWD. Concentrations of DOC were much higher in CWD leachate than in throughfall or litter leachate (15 vs. 0.7 and 1.6 mM, respectively), and greater than reported values for other leachates from within forested ecosystems. Other solutes showed a similar pattern, with inorganic N being an exception. Our results suggest that microsite scale fluxes of DOC from CWD may be An high relative to throughfall and litter leaching fluxes, but since CWD covered a relatively small fraction (2%) of the forest floor in our study, ecosystem scale fluxes from CWD may be negligible for this site. Soil directly beneath CWD may be influenced by CWD leaching, in terms of soil organic matter, microbial activity, and N availability. Concentrations of some metals showed correlations to DOC concentrations, highlighting the possibility of complexation by DOM. Several solute concentrations in throughfall, including DOC, showed positive correlations to mean air temperature, and fewer showed positive correlations in litter leachate, while negative correlations were observed to precipitation, suggesting both biological and hydrologic control of solute concentrations.     

Soil water, nutrient availability and sapling survival under organic and polyethylene mulch in a seasonally dry tropical forest

We examine the effect of mulches on the soil volumetric water content (SVWC), pH, carbon (C), total and mineral (NH₄ and NO₃) nitrogen (N), total and bicarbonate phosphorus (P), and on the survival and relative growth rate of three species, Ipomea wolcottiana Rose, Lonchocarpus eriocarinalis Micheli and Caesalpinia eriostachys Benth, in a degraded seasonally dry tropical forest (SDTF) area. Our study year was unusually dry, with only half of the mean annual rainfall. Sixteen plots (5 × 6 m) for each of our four treatments, mulches with alfalfa (Medicago sativa L.) straw, forest litter (SDTF litter), polyethylene and bare soil (control), were used. In each plot, 20 tree saplings were planted of each species. The SVWC was higher in plots mulched with polyethylene than in bare soil plots. The soil pH did not change with mulching, and there were no differences between treatments in the concentrations of soil organic C, total N, NO₃ and total P. However, soil concentrations of NH₄ were highest in plots with alfalfa straw and of bicarbonate P in plots with polyethylene. Sapling survival was higher in polyethylene mulch plots than in other mulching treatments, in the order I.␣wolcottiana > C. eriostachys > L. eriocarinalis. Sapling survival under organic mulches, alfalfa straw and forest litter were similar, and lowest in bare soil. The relative growth rate followed the order L. eriocarinalis < C. eriostachys < I. wolcotiana, and the growth rate of all species was greatest under polyethylene mulch. We conclude that a combination of polyethylene mulch with species of high growth rate is best for restoring seasonally dry tropical areas.     

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.     

Changes in soil phosphorus fractions following positive and negative phosphorus balances for long periods

The effect of phosphorus (P) balance (addition, in both fertilizers and farmyard manure (FYM), minus removal in crops) on eight soil P fractions determined by sequential extraction, was measured on archived soils from various long-term experiments run by Rothamsted Experimental Station in the United Kingdom. It has been established unequivocally that, for all the soils investigated, no one of the eight P fractions was increased or decreased during long periods of P addition or depletion, respectively. However, changes were mainly in the resin (24–30%) and the inorganic (P_i) component of the four fractions extracted sequentially by 0.5 M NaHCO₃, 0.1 M NaOH, 1.0 M NaOH, 0.5 M H₂SO₄ (41–60%). For the sandy loam there were also consistent changes in the organic (P_o) fraction (25%), especially that extracted by bicarbonate, presumably because the soil contained only a little clay and presumably had low sorption capacity. When the soils were cropped without P addition the largest proportional change was in the P extracted by resin, 0.5 M NaHCO₃ and 0.1 M NaOH, suggesting that the P in these fractions is readily available, or has the potential to become available, for crop growth. This was supported by changes in the overall P balance. On the heavier textured soils, 50–80% of the change in total soil P (P_T) was in these fractions; on the sandy soil this increased to more than 90%. The change in the sum of the first five fractions accounted, on average, for 90% of the P balance. However these changes in the P in the plough layer frequently left large amounts of P unaccounted for in some of the excessively P enriched soils. The amount of P_i extracted by resin and bicarbonate (P_i(r+b)) ranged between 14 and 50% of the sum of the P_i fractions. Soils with the lower percentages were those known to be most responsive to P fertilizers. P_i(r+b) accounted for an average of 70% of the P balance (negative) in P depleting soils where crop offtake was not offset or exceeded by annual P additions (positive balance). The ratio between P_i(r+b) and P_i(sum) could be a guide in defining soils deficient in P and those which are excessively enriched.     

Physiological changes in white lupin associated with variation in root-zone CO2 concentration and cluster-root P mobilization

White lupin (Lupinus albus L.) mobilizes insoluble soil phosphorus through exudation of organic acids from ‘cluster’ roots. Organic acid synthesis requires anaplerotic carbon derived from dark CO₂ fixation involving PEP-carboxylase. We tested the hypothesis that variation in root-zone CO₂ concentration would influence organic acid synthesis and thus P mobilization. Root-zone CO₂ concentrations and soil FePO₄ concentrations supplied to sand-grown white lupin (cv. Kiev Mutant) were varied. More biomass accumulated in plants supplied with 360 µL L⁻¹ CO₂ to the root-zone, compared with those aerated with either 100 or 6000 µL L⁻¹ CO₂. Increased FePO₄ in the sand resulted in greater leaf P concentrations, but root-zone [CO₂] did not influence leaf P concentration. Suppression of cluster-root development in plants supplied with 100 µL L⁻¹ root-zone CO₂ was correlated with increased leaf [P]. However, at both 360 and 6000 µL L⁻¹ CO₂, cluster-root development was suppressed only at the highest leaf P concentration. Phloem sap [P] was significantly increased by greater [FePO₄] in the sand, but was reduced with increased root-zone [CO₂], and this may have triggered increased cluster-root initiation. Succinate was the major organic acid (carboxylate) in the phloem sap (minor components included malate, citrate, fumarate) and was increased at greater [FePO₄], suggesting that this shoot-derived carboxylate might provide an important source of organic acids for root metabolism. Since cluster root development was inhibited by increasing concentrations of FePO₄ in the sand, it is possible that succinate was utilized for the functioning of the root-nodules.     

The influence of tree species on canopy soil nutrient status in a tropical lowland wet forest in Costa Rica

The canopy is host to a large percentage of the flora and fauna in tropical wet forests and is distinct from the forest floor in plant richness, soil type and microclimate. In this study, we examined the influence of tree species and season on soil nutrient cycling processes in canopy soils of four tree species common to Costa Rican wet forests. We also compared the canopy soils to the associated forest floor mineral soils. Both tree species and season had strong effects on canopy soil nutrients and processes. Canopy soils from trees with high litter lignin concentrations had higher net N-mineralization rates and higher dissolved inorganic N concentrations than those with low lignin concentrations. During the dry season, net N-immobilization occurred and dissolved organic and inorganic N and available P concentrations were significantly higher than during the wet season. Overall, canopy soils had higher N levels and higher fungi + bacteria richness than forest floor mineral soils. The differences in canopy soil properties observed among tree species indicates that these species have distinct N cycles that reflect differences in both soil origin and biological controls.     

Recovery of soil phosphorus on former bauxite mines through tropical forest restoration

Soil phosphorus (P) is a major driver of forest development and a critically limited nutrient in tropical soils, especially when topsoil is removed by mining. This nutrient can be present in soils in the form of different fractions, which have direct consequences for P availability to plants and, consequently, for restoration success. Therefore, understanding how the stocks of different soil P fractions change over the restoration process can be essential for guiding restoration interventions, monitoring, and adaptive management. Here, we investigated the recovery of soil P fractions by forest restoration interventions on bauxite mine sites in the Brazilian Atlantic Forest. We assessed the concentration of different fractions of soil organic and inorganic P at (1) a bauxite mine prepared for restoration; (2) two former bauxite mines undergoing forest restoration for 6 and 24 years; and (3) an old‐growth forest remnant. Overall, restored areas recovered levels of labile organic P (P_o‐NaHCO₃) at 5–40 cm and of moderately labile organic P (P_o‐NaOH) at different depths, exhibiting concentrations similar to those found in a conserved forest. The use of P‐rich fertilizers and forest topsoil may have greatly contributed to this outcome. Some other fractions, however, recovered only after 24 years of restoration. Other inorganic P fractions did not differ among mined, restored, and conserved sites: nonlabile P_i (residual P and P‐HCl), labile P_i (P_i‐NaHCO₃), and moderately labile P_i (P_i‐NaOH). Forest restoration was able to promote efficient recovery of important soil P fractions, highlighting the value of restoration efforts to mitigate soil degradation by mining.     

蚂蚁筑巢对西双版纳热带森林土壤有机氮矿化的影响

蚂蚁作为生态系统工程师能够调节土壤微生物及理化环境,进而对热带森林土壤有机氮矿化速率及其时间动态产生显著影响。以西双版纳白背桐热带森林群落为研究对象,采用室内需氧培养法测定土壤有机氮矿化速率,比较蚁巢和非蚁巢土壤有机氮矿化速率的时间动态,揭示蚂蚁筑巢活动引起土壤无机氮库、微生物生物量碳及化学性质改变对有机氮矿化速率时间动态的影响。结果表明：（1）蚂蚁筑巢显著影响土壤有机氮矿化速率（P<0.01）,相较于非蚁巢,蚁巢土壤有机氮矿化速率提高了261%;（2）土壤有机氮矿化速率随月份推移呈明显的单峰型变化趋势,即6月最大（蚁巢1.22 mg kg^-1 d^-1、非蚁巢0.41 mg kg^-1 d^-1）,12月最小（蚁巢0.82 mg kg^-1 d^-1、非蚁巢0.18 mg kg^-1 d^-1）;（3）两因素方差分析表明,不同月份及不同处理对土壤有机氮矿化速率、NH₄-N及NO₃-N产生显著影响（P<0.05）,但对NO₃-N的交互作用不显著;（4）蚂蚁筑巢显著提高了无机氮库（NH₄-N与NO₃-N）、微生物生物量碳、有机质、水解氮、全氮及易氧化有机碳等土壤养分含量,而降低了土壤pH值;（5）回归分析表明,铵态氮和硝态氮对土壤有机氮矿化速率产生显著影响,分别解释87.89%、61.84%的有机氮矿化速率变化;（6）主成份分析表明NH₄-N、微生物生物量碳及有机质是影响有机氮矿化速率时间动态的主要因素,而全氮、NO₃-N、易氧化有机碳、水解氮及pH对土壤有机氮矿化速率的影响次之,且pH与土壤有机氮矿化速率呈显著负相关。总之,蚂蚁筑巢活动主要通过影响土壤NH₄-N、微生物生物量碳及有机质的状况,进而调控西双版纳热带森林土壤有机氮矿化速率的时间动态。研究结果将有助于进一步提高对土壤氮矿化生物调控机制的认识。     

Landscape Controls on Organic and Inorganic Nitrogen Leaching across an Alpine/Subalpine Ecotone,Green Lakes Valley,Colorado Front Range

Here we report measurements of organic and inorganic nitrogen (N) fluxes from the high-elevation Green Lakes Valley catchment in the Colorado Front Range for two snowmelt seasons (1998 and 1999). Surface water and soil samples were collected along an elevational gradient extending from the lightly vegetated alpine to the forested subalpine to assess how changes in land cover and basin area affect yields and concentrations of ammonium-N (NH₄-N), nitrate-N (NO₃-N), dissolved organic N (DON), and particulate organic N (PON). Streamwater yields of NO₃-N decreased downstream from 4.3 kg ha⁻¹ in the alpine to 0.75 kg ha⁻¹ at treeline, while yields of DON were much less variable (0.40–0.34 kg ha⁻¹). Yields of NH₄-N and PON were low and showed little variation with basin area. NO₃-N accounted for 40%–90% of total N along the sample transect and was the dominant form of N at all but the lowest elevation site. Concentrations of DON ranged from approximately 10% of total N in the alpine to 45% in the subalpine. For all sites, volume-weighted mean concentrations of total dissolved nitrogen (TDN) were significantly related to the DIN:DON ratio (R ² = 0.81, P < 0.001) Concentrations of NO₃-N were significantly higher at forested sites that received streamflow from the lightly vegetated alpine reaches of the catchment than in a control catchment that was entirely subalpine forest, suggesting that the alpine may subsidize downstream forested systems with inorganic N. KCl-extractable inorganic N and microbial biomass N showed no relationship to changes in soil properties and vegetative cover moving downstream in catchment. In contrast, soil carbon–nitrogen (C:N) ratios increased with increasing vegetative cover in catchment and were significantly higher in the subalpine compared to the alpine (P < 0.0001) Soil C:N ratios along the sample transect explained 78% of the variation in dissolved organic carbon (DOC) concentrations and 70% of the variation in DON concentrations. These findings suggest that DON is an important vector for N loss in high-elevation ecosystems and that streamwater losses of DON are at least partially dependent on catchment soil organic matter stoichiometry. Received 26 July 2001; accepted 6 May 2002.     

Legacy phosphorus in subtropical wetland soils: Influence of dairy, improved and unimproved pasture land use

Wetlands provide various ecosystem services. One of these services includes nutrient storage in soils. Soils retain and release nutrients such as phosphorus (P). This dynamic can be controlled by soil characteristics, overlying water quality, environmental conditions and historical nutrient loading. Historical nutrient loading contributes to a legacy of P stored in soils and this may influence present day P dynamics between soil and water. We quantified P characteristics of wetland soils and determined the availability and capacity of soils to retain additional P loadings. We sampled surface (0-10) and subsurface (10-30) wetland soils within dairy, improved and unimproved pastures. Surface soils had much greater concentrations of organic and inorganic P. Wetland soils in dairy had greatest concentrations of Ca and Mg, probably due to inputs of inorganic fertilizer. They also had much greater total P, inorganic P, and P sorption capacity; however, these soils were P saturated and had little capacity to retain additional P loading. Improved and unimproved pasture wetland soils had greatest amounts of organic P (>84%) and a capacity to store additional P loadings. Using multivariate statistics, we determined that rather than being different based on land use, wetland soils in improved and unimproved pasture were dissimilar based upon organic matter, organic P fractions, residual P, and soil metal (Fe and Al) content. The legacy of stored P in soils, particularly wetland soils from dairies, combined with best management practices (BMPs) to reduce nutrient loading to these systems, could contribute to a short-term release of soil-stored P to overlying wetland water.     

佛山地区存留自然林和存留人工林的土壤无机磷组分

为探讨热带亚热带森林,尤其城市及其周边地区残存森林土壤磷的有效性,对佛山地区14个残存林(7个自然林和7个人工林)的0~3 cm和3~23 cm矿质土壤的P有效性进行研究。结果表明,铁结合态无机P和还原剂可溶解无机P是土壤无机P的主要组分。在0~3 cm矿质层中,自然林土壤铝结合态无机P、Bray 1提取无机P和总无机P含量显著高于人工林;而在3~23 cm矿质土层中,自然林土壤钙结合态无机P含量显著高于人工林。其它土壤营养指标在自然林和人工林间差异不显著。相关分析结果表明,土壤有机质含量与钙结合态无机P除外的其它无机P组分含量均成显著正相关。聚类分析结果表明14个残存林土壤P有效性可分成3组,整体上人工林土壤P有效性比自然林低。这有助于认识城市化影响下城市及其周边地区残存森林土壤营养状况及加强养分管理。     

Assessment of phosphorus leaching losses from arable land

Phosphorus (P) losses from soil to water by erosion and surface runoff have been much studied and quantified. However, P losses by leaching have received much less attention, mainly because, until recently, the quantities involved were not considered to be of environmental significance. Furthermore, P leaching losses, unlike P losses from erosion or surface runoff were not believed to be related to rates of P addition, as inorganic fertilizer or manures. Here we report results from a number of field and laboratory experiments, designed to assess the significance of P leaching losses from soil to water. Annual cumulative total P losses in drainage waters from four UK field sites ranged from about 0.03 to 5 kg P ha⁻¹ during 2001–2002. Molybdate reactive P ranged from 45–57%, soluble organic P from 10–13% and particulate P from 29–45% of total P on the two sites (Broadbalk and Woburn) where they could be accurately measured. The proportions of these different P forms were comparable in all treatments, including drainage waters from the unfertilised soils and soils receiving long-term applications of farmyard manure or inorganic fertilizer. In all soils, there was indication of an Olsen- (0.5 M NaHC0₃-, pH 8.5) extractable P concentration, (termed the Change-Point), where P measured in field drainage waters or in laboratory soil extracts of 0.01 M CaCl₂ began to increase linearly as Olsen-P increased. There was also some agreement between drainage water-P or CaCl₂-P and the Olsen-P concentration where the Change-Point occurred. This suggests that CaCl₂-extractable P may provide an approximate indicator of soil P concentrations above which significant quantities of P may be lost by leaching under field conditions. There were positive linear relationships between soil dithionate-extractable Al and soil organic C with the Change-Point: [Change Point = [(0.049)[Al3+] minus (9.2)(% organic C)] accounting for 93% of the variance in the data. If this relationship holds under further testing it could well be a useful predictor of Change-Points in different soils. Phosphate sorption isotherms were used to study the soil P concentrations above which P was at risk of moving from soil to water. They showed that soil solution P concentrations were significantly lower between pH 6.9–7.2 than between pH 7.7–8.1, with implications for P loss from soil to water.     

Dissolved organic sulphur in soil water under <Emphasis Type="Italic">Pinus sylvestris</Emphasis> L. and <Emphasis Type="Italic">Fagus sylvatica</Emphasis> L. stands in northeastern Bavaria,Germany variations with seasons and soil depth

Organically bound species have been identified as prominent and mobile forms of nitrogen and phosphorus in soils. Since a large portion of sulphur (S) in soil is bonded to carbon (C) also dissolved organic S likely is a significant constituent in soil water. To investigate the role of dissolved organic forms in leaching and cycling of S in forest soils, we examined concentrations, fluxes, and chemical composition of organic S in forest floor leachates and in soil solutions of Rendzic Leptosols under 90-year-old European beech (Fagus sylvatica L.) and Haplic Arenosols under 160-year-old Scots pine (Pinus sylvestris L.) for 27 months. These soils are low in adsorbed SO₄^2- and receive little atmospheric S depositions at present. The chemical composition of organic S was estimated by fractionation with XAD-8 and wet-chemical characterisation (HI reduction) of binding forms. Although not as prominent as the organic forms of other nutrient elements, organic S proved to be an important contributor to S dissolved in forest floor leachates and in mineral soil solutions. Dissolved organic matter contained on average 29% of total S in forest floor leachates at the pine site and 34% at the beech site. The largest portion of organic S occurred in the subsoil solutions under beech in summer and autumn (up to 53%). Mean concentrations of organic S peaked (up to 1.1 mg l^-1) in summer after rainstorms that followed dry periods. Fluxes with forest floor leachates and at 90 cm soil depth were largest in autumn because of huge amounts of rainfall. Organic S contributed significantly to the fluxes of S in the subsoils under beech comprising on average 39% of total dissolved S at 90 cm depth. Organic S produced in the forest floor layers was mainly in the hydrophilic fraction of dissolved organic matter (62 ± 6% at the pine site, 85 ± 4% at the beech site). The major binding form of organic S in the hydrophobic fraction was C-bonded S while in the hydrophilic fraction ester sulphate S, possibly associated with carbohydrates, was more prominent. Since the hydrophobic fraction increased in summer and autumn, C-bonded S was of greater importance during that time of the year than in winter and spring. With depth, concentrations and composition of organic S (and also of C) hardly changed at the pine site because of little retention of dissolved organic matter, presumably because of the small sorption capability of that soil. At the beech where organic C showed a marked decrease with depth, only a slight decrease in organic S, exclusively from the hydrophobic fraction, was found indicating that organic S was mobile compared with organic C. This was probably due to the concentration of S in the hydrophilic fraction of dissolved organic matter. Because of being concentrated in the mobile hydrophilic fraction, ester sulphate S was more mobile in the soil under beech than C-bonded S.