Influence of Submerged Plants on Phosphorus Fractions and Profiles of Sediments in Gucheng Lake

To understand the effect of submerged macrophytes on P in sediment, P fractions in the surface sediments (0–20 cm) of Potamogeton crispus, Potamogeton maackianus and non-vegetated areas were investigated. In the submerged macrophytes areas, the concentrations of HCl-P, NaOH-P, IP, OP and BD-P were significantly lower than in the non-vegetated area. NH₄Cl-P did not differ significantly among areas.

In the submerged macrophyte distribution areas, TP was significantly correlated with IP and OP. However, in the non-vegetated area, TP was significantly correlated with NH₄Cl-P and OP. In all of the areas sampled, IP was the major phosphorus fraction in the sediments, which consists largely of NAOH-P and HCl-P. The decreasing order of P fractions was: IP > HCl-P > NaOH-P > OP > BD-P > NH₄Cl-P. These results show that submerged macrophytes can decrease the concentrations of all P fractions and imply that submerged macrophytes play a key role in the retention of P nutrients.     

Longitudinal Variability of Phosphorus Fractions in Sediments of a Canyon Reservoir Due to Cascade Dam Construction: A Case Study in Lancang River,China

Dam construction causes the accumulation of phosphorus in the sediments of reservoirs and increases the release rate of internal phosphorus (P) loading. This study investigated the longitudinal variability of phosphorus fractions in sediments and the relationship between the contents of phosphorus fractions and its influencing factors of the Manwan Reservoir, Lancang River, Yunnan Province, China. Five sedimentary phosphorus fractions were quantified separately: loosely bound P (ex-P); reductant soluble P (BD-P); metal oxide-bound P (NaOH-P); calcium-bound P (HCl-P), and residual-P. The results showed that the total phosphorus contents ranged from 623 to 899 µg/g and were correlated positively with iron content in the sediments of the reservoir. The rank order of P fractions in sediments of the mainstream was HCl-P>NaOH-P>residual-P>BD-P>ex-P, while it was residual-P>HCl-P>NaOH-P>BD-P>ex-P in those of the tributaries. The contents of bio-available phosphorus in the tributaries, including ex-P, BD-P and NaOH-P, were significantly lower than those in the mainstream. The contents of ex-P, BD-P, NaOH-P showed a similar increasing trend from the tail to the head of the Manwan Reservoir, which contributed to the relatively higher content of bio-available phosphorus, and represents a high bio-available phosphorus releasing risk within a distance of 10 km from Manwan Dam. Correlation and redundancy analyses showed that distance to Manwan Dam and the silt/clay fraction of sediments were related closely to the spatial variation of bio-available phosphorus.     

The spatio-temporal variations of sedimentary phosphorus in Taihu Lake and the implications for internal loading change and recent eutrophication

Internal phosphorus loading is particularly concerned for the shallow lakes due to the frequent sediment disturbance, which may play a vital role in changing nutrient level in overlying water. A historical perspective on internal phosphorus loading may contribute to understanding its contribution to recent eutrophication. In this work, a study on the changes in internal phosphorus loading and release potential in Taihu Lake, a shallow eutrophic lake in China, was performed based on the analysis of spatio-temporal variations of sedimentary total phosphorus and three operationally defined fractions (NaOH-P, HCl-P and OP). The influencing factors for changing internal loading were discussed. The results showed that internal phosphorus loading was elevated compared to pre-eutrophication periods and the increase has occurred since approximately the late 1970s to early 1980s. Changes in internal phosphorus loading were primarily attributed to the NaOH-P and OP fractions, relating to anthropogenic inputs and enhanced productivity, respectively. The internal phosphorus release potential may be enhanced by up to 22% currently relative to the pre-eutrophication period; however, it should play a secondary role to external input in enhancing nutrient levels and sustaining the eutrophication in Taihu Lake.     

Fractional phosphate composition in sediments from a tropical river (Catatumbo River, Venezuela)

The distribution of phosphate species in the Catatumbo River, Venezuela, was studied using a sequential extraction scheme. Extraction was performed using 1.0 M NH₄Cl, 0.1 M Na₂S₂O₄–NaHCO₃, 1.0 M NaOH and 0.5 M HCl. Total phosphate was in the range between 121 and 581 g g^–1 D.W. About 64% of the total phosphate is inorganic and present the following composition: 1% NH₄Cl-P, 10% BD-P, 20% NaOH-P, 33% HCl-P; while org-P is 36%. The main form of P in sediment from the Catatumbo River is calcium bound-P, like apatite. The metal concentrations present in sediment are in the following order: Fe> Al > Ca > Mg > Mn. Relationships between P and Fe, Al and Ca were found. Cluster analysis showed that speciation is not dependent on the inorganic matrix of the sediments. Analysing the influence of NaOH concentration and duration of the extraction invalidated the use of NaOH as extracting agent in P-speciation.     

Vertical distribution and release characteristics of phosphorus forms in the sediments from the river inflow area of Dianchi Lake,China

Columnar sediment samples were collected from five representative river inflow areas of Dianchi Lake, China. The vertical distribution of each form of P were tested. Results showed that the concentration of TP in the sediments from areas A, B, C, D and E in the order of D > B > A > C > E, and the average concentration of D, B, A, C and E were 2991, 2064, 1308, 879, and 759 mg?kg^?1, respectively. The concentration of Ex-P, Fe/Al-P, Ca-P and Org-P all decreased with increasing depth. The release of Ex-P was significantly related to TP whereas the Fe/Al-P was not significantly related to TP in the samples from areas polluted by domestic sewage. However, the release of Ex-P and Fe/Al-P were both significantly related to TP in the samples from areas polluted by phosphate mining and phosphate fertilizer application. The results of equilibrium P concentration (EPC0) analysis showed that P in the sediments of areas A, D and E were the source of P in Dianchi Lake, and the P in the sediments of areas B and C were in relative equilibrium with the overlying water.     

Adsorption of Antimony on Sediments from Typical Water Systems in China: A Comparison of Sb(III) and Sb(V) Pattern

The present work investigated the adsorption of Sb(III) and Sb(V) on five sediment samples (Pearl River, Yangtze River, Yellow River, Yongding River, and Liao River) from typical water systems in China and the adsorption of Sb(V) on Pearl River sediment with different organic carbon (OC) fractions using batch experiments. In order to assess the contributions of sedimentary organic components to the overall adsorption of pentavalent Sb on sediments, one sediment sample was treated by commonly used chemical and physical methods to remove different organic components. Experimental data of Sb(III) and Sb(V) adsorption on five sediments were successfully modeled using the Freundlich (r² > 0.96) isotherm. In general, the sediments with high Fe and Al oxide contents and total organic carbon (TOC) had higher Sb(III) and Sb(V) adsorption than the sediments containing small amounts of Fe and Al oxides and TOC. Dissolved organic carbon (DOC) in sediment promoted the adsorption of Sb(V), and humin fractions and black carbon-like material in sediment had a high affinity for Sb(V).     

From sediment to soil: floodplain phosphorus transformations at the Danube River

Substantial transformations of biogeochemical phosphorus (P) fractions can occur within a few hundreds of years under humid and tropical conditions; however, slower changes are expected under dry and temperate climate. The objective of this study was to infer P transformations over time by comparing suspended sediments in the Danube River to floodplain soils developed from such sediments over different time periods in the continental climate of Central Europe. We analyzed suspended sediments from 20 flood events between 1990 and 2006, and floodplain soils from seven sites along a chronosequence covering about 500 yrs. The studied flood sediments had similar characteristics over the 16-yr observation period. Total phosphorus (TP) averaged 732 mg kg⁻¹, and biogeochemical fractionation yielded important primary mineral contributions (apatite phosphorus, AP, ~80% of TP). The TP concentrations of the floodplain soils were in the range of the Danube sediments and showed little variation along the chronosequence. However, the distribution of P among biogeochemical fractions changed considerably in less than 500 yrs of soil development. The youngest soils (<20 yrs) were dominated by AP, as was observed for the Danube sediments. In less than 250 yrs of pedogenesis, AP markedly decreased and organic phosphorus (OP) increased, and in less than 500 yrs, OP reached AP levels. This shows that while P biogeochemistry in very young floodplain soils is strongly related to the river sediments, significant transformations can occur in less than 250 yrs of soil development in the dry and temperate climate of Central Europe.     

Variability of the sediment phosphate composition of a temporary pond (Doñana National Park,SW Spain)

This study reports on the spatial and temporal variability of the phosphate composition in the sediment of a temporary pond over a period of 3 years using the EDTA-method for P-fractionation. Sediment samples were collected at three different sites (open-water, littoral and flood plain) to compare the effect of the length of the wet/dry phase on the sediment phosphate composition, with special emphasis on the potential bioavailability of the P-fractions.Fine sediments (<0.1 mm) were rich in organic matter (9–25%) and contained high mean concentrations of Tot-P (182–655 mg kg^–1 d.w.), especially in the flood plain sediment. The sediment P composition was dominated by P-organic fractions at all sites (64–94%). The average C/N ratios were 8.8, 6.0 and 5.9 for sediments of the flood plain, littoral and open-water sites, respectively. The flood plain sediment was significantly poorer in iron-bound P (FeOOHP), but richer in the P-organic fractions extracted by EDTA than the sediment of the open-water site (P<0.01). The percentage of organic matter increased significantly in the sediment of the open-water site at the end of each dry season (P<0.05), while it decreased in the sediment of the flood plain site (P<0.01). In all sediments, the fraction of Fe(OOH)P decreased at the end of each dry season and some of these changes were significant (P<0.05). The decrease in the fraction of Fe(OOH)P was not related to changes in the sediment redox potential. Although the flood plain site was dry longer than the open-water site during the study period, the differences between the sediment composition of both sites were probably due to the effect of plant growth on the dry sediments of the flood plain site rather than to a direct effect of desiccation.     

The chemical character and burial of phosphorus in shallow coastal sediments in the northeastern Baltic Sea

The chemical composition and vertical distribution of sediment phosphorus (P) in shallow coastal sediments of the northeastern Baltic Sea (BS) were characterized by sequential extraction. Different P forms were related to chemical and physical properties of the sediments and the chemistry of pore water and near-bottom water. Sediment P composition varied among the sampling sites located in the Archipelago Sea (AS) and along the northern coast of the Gulf of Finland (GoF): the organic rich sites were high in organic P (OP), while apatite-P dominated in the area affected by sediment transportation. Although the near-bottom water was oxic, the sediments released P. Release of P was most pronounced at the site with high sediment OP and reduced conditions in the sediment-water interface, indicating that P had its origins in organic sources as well as in reducible iron (Fe) oxyhydroxides. The results suggest that even though these coastal areas are shallow enough to lack salinity stratification typical for the brackish BS, they are vulnerable to seasonal oxygen (O₂) depletion and P release because of their patchy bottom topography, which restricts mixing of water. Furthermore, coastal basins accumulate organic matter (OM) and OP, degradation of which further diminishes O₂ and creates the potential for P release from the sediment. In these conditions, an abundance of labile OP may cause marked efflux of P from sediment reserves in the long-term.     

Changes in microbial biomass and P fractions in biogenic household waste compost amended with inorganic P fertilizers

The present study was conducted to evaluate the changes in microbial biomass indices (C, N, and especially P) and in P fractions in compost amended with inorganic P fertilizers. In the non-amended control, the average contents of microbial biomass C, N, and P were 1744, 193, and 63 microg g(-1) compost, respectively. On average, 1.3% of total P was stored as microbial biomass P. The addition of KH(2)PO(4) and TSP (triple super phosphate) led to immediate significant increases in microbial biomass C, N, and P. Approximately, 4.6% of the added TSP and 5.8% of the added KH(2)PO(4) were incorporated on average into the microbial biomass throughout the incubation. Approximately, 4.7% of the 1mg and 5.8% of the 2mg addition rate were incorporated on average into the microbial biomass. In the amendment treatments, the average contents of microbial biomass C, N, and P declined by 44%, 64%, and 49%, respectively. Initially, the average size of the P fractions in the non-amended compost increased in the order (% of total P in brackets) resin P (0.7%)相似文献   

Influence of redox potential on phosphate-uptake by sediments in two sub-tropical eutrophic lakes

Biogeochemical reactions in shallow eutrophic lakes areaffected bythe changes in redox potential (Eh) as bottom sedimentsundergotemporal resuspension and settling. The stability of varioussediment P fractions and kinetics of P-uptake were evaluatedfortwo sub-tropical lakes (Lake Apopka and Lake Okeechobee,Florida)using sediment suspensions in closed systems maintained atvariousEh levels ranging from –235 to 555 mV. Redox potential hadminimal effect on the stability of NaOH-P (Fe-/Al-bound P plusmoderately resistant organic P) and HCl-P (Ca-/Mg-P) fractionsinLake Apopka sediments. Increases in ortho-P and NH₄Cl-P(loosely-bound P plus labile organic P) concentrations wereobserved in highly reduced (Eh=–225 mV) Apopkasediments.Phosphate solubility diagrams and mineral equilibriacalculationssuggest that P-uptake by Apopka bottom sediments at elevated Pconcentrations (ortho-P110 M) was due toformationof Ca-P compounds and/or co-precipitation of P withCaCO₃. Incontrast, the ortho-P concentrations for Lake Okeechobeebottomsediments increased exponentially with decreasing Eh. Thequantityof NaOH-P fractions for these sediments decreased withdecreasingEh, suggesting the release of Fe- and Mn-bound P intosolution.Phosphate-uptake by Okeechobee bottom sediments (pH 7.5,ambient)followed first order kinetics, yielding a rate constant (k)of 0.51±0.05 h^-1. Unlike that of Apopka, the mudsediments in Lake Okeechobee have strong affinity for P ineitheraerobic or anaerobic conditions. Results suggest that even incalcareous systems, Fe and Al, when present in highconcentrations(as in the case of Lake Okeechobee), are actively involved inregulating P-uptake and geochemistry.     

Enzymatic hydrolysis of organic phosphorus in river bed sediments

Enzymatic hydrolysis of phosphorus (P) in bed sediments is an important process that maintains bioavailable P in the river systems. The P bioavailability is the criterion for assessing the eutrophication potential in rivers and streams. The objective of this research was to determine potential bioavailability of organic P (OP) in the Bronx River bed sediments using native phosphatases (NPase) and phosphodiesterase (PDEase) hydrolysis. The bed sediments collected in summer 2006 and 2007 were incubated at 37 °C for 6 h at pH 7.5 with NPase. The results showed that NPase hydrolyzed a substantial amount of OP (up to 76%) under favorable temperature and pH, indicating OP could be hydrolyzed under increased temperature, and in turn increase in P availability in the river. Similarly, the resulting form sediments incubated with PDEase at 37 °C and pH 8.8 showed that up to 82% of OP could be hydrolyzed. Strong correlations between percentage of OP hydrolyzed by PDEase and organic matter (OM) were observed for sediments collected in 2006 (r = 0.745; p ≤ 0.01) and 2007 (r = 0.724; p ≤ 0.01), indicating PDEase hydrolysable P is mainly associated with OM. It is indicative that local hydro-climatic changes such as temperature increase and pH variations could hydrolyze a substantial amount of OP and increase bioavailable P in the water column, resulting in a potential threat to the river ecosystems.     

Eight years of internal phosphorus loading and changes in the sediment phosphorus profile of Lake Søbygaard,Denmark

During each of the first 8 years following an 80–90% reduction in external phosphorus loading of shallow, hypertrophic Lake Søbygaard, Denmark in 1982, phosphorus retention was found to be negative. Phosphorus release mainly occurred from April to October, net retention being close to zero during winter. Net internal phosphorus loading was 8 g P m^–2 y^–1 in 1983 and slowly decreased to 2 g P m^–2 y^–1 in 1990, mainly because of decreasing sediment phosphorus release during late summer and autumn. The high net release of phosphorus from Lake Søbygaard sediment is attributable to a very high phosphorus concentration and to a high transport rate in the sediment caused by bioturbation and gas ebullition. Sediment phosphorus concentration mainly decreased at a depth of 5 to 20 cm, involving sediment layers down to 23 cm. Maximum sediment phosphorus concentration, which was 11.3 mg P g^–1 dw at a depth of 14–16 cm in 1985, decreased to 8.6 mg P g^–1 dw at a depth of 16–18 cm in 1991. Phosphorus fractionation revealed that phosphorus release was accompanied by a decrease in NH₄Cl-P + NaOH-P and organic phosphorus fractions. HCl-P increased at all sediment depths. The Fe:P ratio in the superficial layer stabilized at approximately 10. Net phosphorus release can be expected to continue for another decade at the present release rate, before an Fe:P ratio of 10 will be reached in the sediment layers from which phosphorus is now being released.     

Phosphorus speciation in Myall Lake sediment, NSW, Australia

The amount of phosphorus and its fractions in the sediment of Lake Myall, NSW, Australia, was assessed using a sequential extraction technique. Five sedimentary phosphorus reservoirs were measured, namely loosely sorbed phosphorus (NH₄Cl–P), iron associated phosphorus (BD–P), calcium bound phosphorus (HCl–P), metal oxide bound phosphorus (NaOH–P) and residual phosphorus (organic and refractory P, Res-P). Samples were taken from the deep and shallow sites of the lake. During the analysis, the average concentrations of each fraction of phosphorus was calculated. The results depicted that the total phosphorus (TP) content and chemically extractable phosphorus in both fine and coarse sediment fractions from the deep sites of the lake were significantly higher than those of the shallow sites, except for HCl–P extracted from the fine sediment fraction. Sediment TP was also strongly and positively correlated to sediment Fe. The phosphorus in the sediment mainly consisted of BD–P and Res-P, while NH₄Cl–P and HCl–P only contributed a minor part. The rank order of the different phosphorus extracts was similar for the two sites, namely Residual-P > BD–P > NaOH–P > HCl–P > NH₄Cl–P.     

Basin-scale comprehensive assessment of cadmium pollution,risk, and toxicity in riverine sediments of the Haihe Basin in north China

A comprehensive and detailed investigation of cadmium (Cd) pollution in surface riverine sediments of the Haihe Basin in north China was carried out. Total Cd concentrations in these sediments ranged from 0.153 to 22.1 mg/kg, exceeding the soil background value at all sampling sites. The mean Cd concentration of the bioavailable fraction was 0.557 mg/kg, accounting on average for 51.58% of the total Cd. A mean value of the Cd enrichment factor of 11.6 suggested that Cd has accumulated in most riverine sediments, resulting in a high degree of anthropogenic pollution. In fact, there were high levels of Cd pollution in the riverine sediments throughout the Haihe Basin, yielding geo-accumulation index values for Cd from 0.071 to 7.25. According to the potential ecological risk index, risk assessment code, and consensus-based sediment quality guidelines, Cd was a serious pollutant in this ecosystem. Because it occurred as a high proportion in the exchangeable/acid soluble fraction (21.21% on average), it may also have biological toxicity. Our findings indicated that it is important to consider Cd in control strategies for managing riverine sediment pollution in the Haihe Basin.     

The role of sediment organic matter composition in larval habitat selection by the polychaete Capitella sp. I

The role of sediment organic matter composition in larval habitat selection by the polychaete Capitella sp. I was investigated using a still water multiple-choice experiment. Specifically, the following question was addressed: what are the roles of sediment labile organic compounds in larval habitat selection? A replicated Latin-square design was used to test larval preferences among sediments collected from five sites (TLC—Tung Lung Chau; VHE—Victoria Harbor east; VH—Victoria Harbor; VHW—Victoria Harbor west; PC—Peng Chau) in the vicinity of Victoria Harbor, Hong Kong. Although mean grain size was not different among sites, water content and the total organic matter were higher in VH Mud but were similar among other sites. Carbohydrate, lipid, and biopolymeric fractions followed the same trend. According to protein content, sites were ranked as: VH > VHW > TLC = VHE > PC. PC Mud had the highest carbohydrate/protein ratio, due to low concentration of protein. According to larval preference, sites were ranked as: TLC = VH = VHW = VHE > PC. Our study shows a precise relationship between sediment biochemical properties and larval habitat selection. Larvae tend to choose sediments with low carbohydrate/protein ratio. Results suggest that types of sediment organic matter may play more important role in the larval habitat selection process of Capitella sp. I than concentration of organic matter alone.     

Phosphorus sorption characteristics of the Bronx River bed sediments

Abstract

Phosphorus (P) is a major nutrient for plant growth, and it is often the primary limiting nutrient in freshwater ecosystems controlling algal blooms. The Bronx River of New York City, New York, USA includes freshwater and coastal water systems. The water quality of both fresh and saline water is lower than the standard levels designated by New York State, and classified as Class B and Class I waters, respectively. Algal blooms and oxygen depletion within the river have degraded the water quality, endangered fishing, and limited recreational use. The internal loading of P, an important bioavailability indicator in the Bronx River, is determined by the sorption processes, i.e., cycling of P between solid and liquid phases. The objectives of this study were to understand how P sorption characteristics affect the internal loading of P and the conditions that might give rise to a flux of P from sediment to the water column, and to estimate the effects of physicochemical properties of the sediments on P sorption parameters. Bed sediments were collected from 15 sites along the Bronx River, from the origin in Westchester Davis Brook, Kensico Dam through the Bronx to the Sound View Park estuary. Phosphorus sorption maximum (S_max) were significantly correlated with oxalate–extractable iron (Ox–Fe) and aluminum (Ox–Al), acid-extractable calcium (HCl–Ca) and magnesium (HCl–Mg), and total organic matter (OM), suggesting that not only metal ions affected P sorption characteristics, but OM also influenced the P sorption processes. This study also showed that originally sorbed P (S₀) was significantly correlated with Ox–Fe, Ox–Al, HCl–Mg, and OM. The extremely high values of the percentage of sorbed P retained in sediments (>98% for all sites except the two estuary sites: site 13 of 88% and site 14 of 92%) suggest that a large flux of P to the water column from the sediments could potentially occur under changing hydro-climatic conditions, such as the changes in pH, ionic strength and redox conditions, which may, in turn, exacerbate eutrophic conditions and subsequent algal blooms.     

Surficial sediment phosphorus fractions along a biogeochemical gradient in Nyanza (Winam) Gulf, northeastern Lake Victoria and their possible role in phosphorus recycling and internal loading

Different phosphorus fractions and metal element composition of surficial sediments were measured on three occasions in 2005 and 2006 along a transect between Nyanza Gulf and offshore Lake Victoria, in order to assess the potential for sediments to contribute to the water column P concentrations in Lake Victoria. Total phosphorus (TP), apatite phosphorus (AP), inorganic phosphorus (IP) and organic phosphorus (OP) increased in sediments along the gulf towards the main lake while the non-apatite inorganic phosphorus (NAIP) increases were less defined. The longitudinal gradient of sediment TP and its fractions in Nyanza Gulf is a result of high rates of terrigenous input and resuspension and transport of the light, phosphorus rich inorganic and organic matter towards the main lake. TP in the sediment ranged from 812.7 to 1,738 mg/kg dry weight (DW) and was highest in the Rusinga Channel, the exchange zone between the gulf and the main lake. AP was the most important TP fraction, contributing between 35 and 57.3% of TP. Ca content in the sediment was strongly associated with TP and AP in the sediment (r² = 0.92 and 0.98, respectively) in the gulf and the channel, indicating the importance of apatite in controlling P availability in these zones. In the gulf and the Rusinga Channel, the less bioavailable apatite phosphorus dominated, whereas in the deeper main lake OP was the major fraction illustrating the importance of anaerobic release of P from sediments and acceleration of internal P loading in the main lake.     

The National Distribution Pattern and Factors Affecting Heavy Metals in Sediments of Water Systems in China

Heavy metal discharge has become one of the most serious environmental problems due to extensive industrialization. Sixty eight sediment samples from four wetlands were collected to analyze the regional factors affecting metal deposition. Meanwhile, a national sediment data collection based on relevant publications was developed covering the period from 2000 to 2016 to study the metal distribution in China. Principal metals assessed in this study are Cr, Cd, Cu, Pb, Zn, As, and Ni. At regional scale, the accumulation of Pb and Cd is significantly higher in surface than in subsurface sediments. At the national scale, heavy metals tend to increase with the increase in precipitation from 600 to 1500 mm. Further, metal deposition in the main river basins in China shows an increase trend from northern to southern China, and follows the order of: Pearl River > Yangste River > Yellow River > Hai River and Liao River. Cluster analyses show that these river basins contribute a large proportion of heavy metals to coastal metal deposition, which follows the order of: South Sea > East Sea > Bohai Sea > Yellow Sea. In general, metal deposition in sediments of water systems increases from northern to southern China irrespective of in-land area or coastal seas.     

Spatial patterns of P fractions and chemical properties in soils of two native shrub communities in Senegal

Two shrub species (Piliostigma reticulatum (D.C.) Hochst (Caesalpinioideae) and Guiera senegalensis J.F. Gmel (Combretaceae) are commonly found in farmers’ fields at varying densities in semi-arid Senegal and throughout the Sahel where soils have chronically low phosphorus (P) availability. It seems plausible that shrub litter and the rhizospheres could influence P fractions and other chemical soil properties that affect crop productivity. Thus, a study was done at two sites, on the distribution of inorganic and organic soil P pools, organic C levels, and pH in soil beneath and outside the canopies of P. reticulatum and G. senegalensis (0-30 cm depth). Both sites had low total P ranging from 64 mg P kg^?1 to 135 mg P kg^-1, and low extractable PO₄ (resin Pi) (1–6 mg P kg^?1) with P fractions dominated by NaOH-P. Organic P (Po) made up about 50% of total P, and most of the organic P (>60%) was found in the NaOH-P fractions. The labile P, particularly bicarb-Po was higher in soil beneath shrub canopies (8.4 mg P kg ^?1), than outside the canopy (6.2 mg P kg ^?1). Similarly, C, N and P to a lesser extent, were more concentrated beneath shrub canopies. P. reticulatum soil was dominated by the NaOH-Po fraction, whereas G. senegalensis had higher bicarb-Po at one of the study sites. An index of biologically available organic P (Bicarb-Po) / (Bicarb-Po?+?Bicar-Pi?+?Resin Pi) was ?>?60% and indicates that biological processes represent an important part of P cycling in these shrub ecosystems. The differential ability of shrubs in modifying soil chemical properties under their canopies has major implications for biogeochemical cycling of nutrients and C in sandy soils of semi arid Sahelian ecosystems.