钙、铁、铝形态对岩溶石灰土磷有效性的影响

为揭示钙、铁、铝形态与岩溶地区土壤磷有效性关系,通过改进的BCR元素形态连续提取法获取石灰土不同发育阶段土壤矿质元素赋存形态,并分析与总磷及速效磷含量之间的相关关系。初步研究表明:石灰土壤中全磷和速效磷在石灰土发育过程呈降低趋势,从黑色石灰土到黄色石灰土,总磷降低了76.7%,速效磷减少了84.7%。石灰土总磷与速效磷同酸溶态、可还原态及残渣态钙,可氧化态铁、铝和可还原态铝显著正相关,而同总铁、总铝以及残渣态铝显著负相关,相关系数绝对值均达到0.9以上。随着石灰土发育进行,钙总量及其形态均降低,而铝、铁总量和形态呈增加趋势,可能导致岩溶地区石灰土磷及其有效性缺乏越发突出。      

Phosphorus distribution in sediments of the Delaware River estuary

In order to determine the primary factors related to the accumulation of phosphorus in estuarine sediments, a study of phosphorus fractions in sediments of the Delaware River Estuary was undertaken. A correlation matrix between the phosphorus fractions, determined by serial extraction, and 14 sediment variables was computed. Total phosphorus and total inorganic phosphorus in the sediment-phosphorus reservoir decreases with increasing salinity. This variation is correlated with decreasing iron oxyhydroxide content in the sediment. Neither clay content nor calcium carbonate content appear to be significantly correlated with variation in total inorganic phosphorus content in the fine-grained sediments of this estuary. Although calcium phosphate is concluded to be a major constituent of the sediment-phosphorus reservoir, there was no evidence found that it is authigenic in this environment.     

Dissolved organic phosphorus speciation in the waters of the Tamar estuary (SW England)

The speciation of dissolved organic phosphorus (DOP) in the temperate Tamar estuary of SW England is described. Eight stations from the riverine to marine end-members were sampled during four seasonal campaigns in 2007 and the DOP pool in the water column and sediment porewater was characterized and quantified using a flow injection manifold after sequential enzymatic hydrolysis. This enabled the enzymatically hydrolysable phosphorus (EHP) fraction and its component labile monoester phosphates, diester phosphates and a phytase-hydrolysable fraction that includes myo-inositol hexakisphosphate (phytic acid), to be determined and compared with the total DOP, dissolved reactive phosphorus (DRP) and total dissolved phosphorus (TDP) pools. The results showed that the DOP pool in the water column varied temporally and spatially within the estuary (1.1-22 μg L⁻¹) and constituted 6-40% of TDP. The EHP fraction of DOP ranged from 1.1-15 μg L⁻¹ and represented a significant and potentially bioavailable phosphorus fraction. Furthermore the spatial profiles of the three components of the EHP pool generally showed non-conservative behavior along the salinity gradient, with apparent internal estuarine sources. Porewater profiles followed broadly similar trends but were notably higher at the marine station throughout the year. In contrast to soil organic phosphorus profiles, the labile monoester phosphate fraction was the largest component, with diester phosphates also prevalent. Phytic acid concentrations were higher in the lower estuary, possibly due to salinity induced desorption processes. The EHP fraction is not commonly determined in aquatic systems due to the lack of a suitable measurement technique and the Tamar results reported here have important implications for phosphorus biogeochemistry, estuarine ecology and the development of efficient strategies for limiting the effects of phosphorus on water quality.     

Phosphorus Mobilization at the Sediment–Water Interface in Softwater Shield Lakes: the Role of Organic Carbon and Metal Oxyhydroxides

The adsorption of phosphorus on natural diagenetic iron (Feox) and manganese (Mnox) oxyhydroxides was studied in deep and littoral zone sediments of mesotrophic Lac Saint-Charles (46°56 N, 71°23 W), using a Teflon sheet technique for collecting diagenetically produced metal oxyhydroxides. Collected metal oxide amounts were greater at the deep-water station, relative to littoral zone stations reflecting sediment and local diagenetic differences. Two-layer surface complexation modeling on iron oxyhydroxide was consistent with the measured total P/Fe molar ratios except for the upper mixed Mn–Fe oxide layer from the littoral stations, where measured phosphorus exceeded the modeled phosphorus by more than fivefold. Soluble reactive phosphorus (SRP) exchange between oxyhydroxide samples and natural lake water in the laboratory revealed a labile phosphorus pool. Phosphorus determined on the Teflon sheets from the littoral zone stations appears to be related to a distinct non-humic organic carbon pool that readily exchanges SRP, while little exchange was observed from material collected from the deep-water station. We suggest that the enhanced SRP release from littoral zone sediments is due to an organic carbon and/or metal oxide-impoverished sediment matrix, limiting microbial oxide reduction and allowing phosphorus to be rapidly recycled at the sediment–water interface, instead of being slowly incorporated into humic material. The SRP fluxes revealed in our study, which originate from the solid phase at the sediment–water interface, would be difficult to resolve using interstitial pore-water samplers and might be a quantitatively important source of inorganic phosphorus in Shield lakes.     

Sediment and Nutrient Deposition Associated with Hurricane Wilma in Mangroves of the Florida Coastal Everglades

The distribution of mangrove biomass and forest structure along Shark River estuary in the Florida Coastal Everglades (FCE) has been correlated with elevated total phosphorus concentration in soils thought to be associated with storm events. The passage of Hurricane Wilma across Shark River estuary in 2005 allowed us to quantify sediment deposition and nutrient inputs in FCE mangrove forests associated with this storm event and to evaluate whether these pulsing events are sufficient to regulate nutrient biogeochemistry in mangrove forests of south Florida. We sampled the spatial pattern of sediment deposits and their chemical properties in mangrove forests along FCE sites in December 2005 and October 2006. The thickness (0.5 to 4.5 cm) of hurricane sediment deposits decreased with distance inland at each site. Bulk density, organic matter content, total nitrogen (N) and phosphorus (P) concentrations, and inorganic and organic P pools of hurricane sediment deposits differed from surface (0–10 cm) mangrove soils at each site. Vertical accretion resulting from this hurricane event was eight to 17 times greater than the annual accretion rate (0.30 ± 0.03 cm year⁻¹) averaged over the last 50 years. Total P inputs from storm-derived sediments were equivalent to twice the average surface soil nutrient P density (0.19 mg cm⁻³). In contrast, total N inputs contributed 0.8 times the average soil nutrient N density (2.8 mg cm⁻³). Allochthonous mineral inputs from Hurricane Wilma represent a significant source of sediment to soil vertical accretion rates and nutrient resources in mangroves of southwestern Everglades. The gradient in total P deposition to mangrove soils from west to east direction across the FCE associated with this storm event is particularly significant to forest development due to the P-limited condition of this carbonate ecosystem. This source of P may be an important adaptation of mangrove forests in the Caribbean region to projected impacts of sea-level rise.     

Phosphorus fractionation in sediments of the Pichavaram mangrove ecosystem,south-eastern coast of India

Present study examined phosphorus dynamics through delineation of source as well as availability of phosphorus and its fractionation within the intertidal sediments of Pichavaram mangrove ecosystem. Twelve sediment samples and two cores were collected from the mangrove forest along with estuarine area (Vellar-Coleroon) during January 2005. Sediments were analyzed for total phosphorus and its fractionation using operationally defined chemical sequential extraction scheme (SEDEX). Dissolved phosphorus (in water) and total phosphorus (in sediments) concentrations were high in the Vellar region of Pichavaram mangrove area due to pollution load from nearby villages and agricultural fields. However, the spatial variation in dissolved phosphorus were insignificant (at significance level = 0.05). The results for the phosphorus fractionation (post-tsunami) were compared with earlier studies (pre-tsunami). It was observed that all phosphorus fractions (except adsorbed-phosphorus) showed a highly significant (at significance level = 0.05) increase in concentration after the tsunami event. There was significant decrease in the adsorbed phosphorus concentration as a result of tsunami. The changes were more pronounced for organic phosphorus which increased by almost twofold following the event. These variations were attributed to change in salinity, increase in dissolved oxygen as well as the retreat of tsunami water carrying the waste load. The vertical distribution of phosphorus through core sediments showed that mixing after tsunami had altered the different phosphorus fraction and its availability. Overall, the study indicated that the fluvial weathering along with litter degradation and anthropogenic sources controlled the biogeochemistry of phosphorus in this mangrove ecosystem. Observed changes in the concentrations are a result of altered physico-chemical characteristics caused by tsunami.     

Nutrient flux in a landscape: Effects of coastal land use and terrestrial community mosaic on nutrient transport to coastal waters

Long-term interdisciplinary studies of the Rhode River estuary and its watershed in the mid-Atlantic coastal plain of North America have measured fluxes of nitrogen and phosphorus fractions through the hydrologically-linked ecosystems of this landscape. These ecosystems are upland forest, cropland, and pasture; streamside riparian forests; floodplain swamps; tidal brackish marshes and mudflats; and an estuarine embayment. Croplands discharged far more nitrogen per hectare in runoff than did forests and pastures. However, riparian deciduous hardwood forest bordering the cropland removed over 80 percent of the nitrate and total phosphorus in overland flows and about 85 percent of the nitrate in shallow groundwater drainage from cropland. Nevertheless, nutrient discharges from riparian forests downslope from croplands still exceeded discharges from pastures and other forests. The atomic ratio of nitrogen to phosphorus discharged from the watersheds into the estuary was about 9 for total nutrients and 6 for inorganic nutrient fractions. Such a low N:P ratio would promote nitrogen rather than phosphorus limitation of phytoplankton growth in the estuary. Estuarine tidal marshes trapped particulate nutrients and released dissolved nutrients. Subtidal mudflats in the upper estuary trapped particulate P, released dissolved phosphate, and consumed nitrate. This resulted in a decrease in the ratio of dissolved inorganic N:P in the estuary. However, the upper estuary was a major sink for total phosphorus due to sediment accretion in the subtidal area. Bulk precipitation accounted for 31 percent of the total nongaseous nitrogen influx to the landscape, while farming accounted for 69 percent. Forty-six percent of the total non-gaseous nitrogen influx was removed as farm products, 53 percent either accumulated in the watershed or was lost in gaseous forms, and 1 percent entered the Rhode River. Of the total phosphorus influx to the landscape, 7 percent was from bulk precipitation and 93 percent was from farming. Forty-five percent of the total phosphorus influx was removed as farm products, 48 percent accumulated in the watershed, and 7 percent entered the Rhode River. These nitrogen and phosphorus discharges into the Rhode River, although a small fraction of total loadings to the watershed, were large enough to cause seriously overenriched conditions in the upper estuary.     

Evaluation of phosphorus bioavailability in sediments of the shallow lakes in the middle and lower reaches of the Yangtze River region,China

Phosphorus (P) fractions and their bioavailability in the sediments from the middle and lower reaches of the Yangtze River region were investigated using different chemical extraction methods. The results show that the contents of bioavailable P in the sediments extracted by different extraction procedures varied greatly. But their rank order was similar. Potentially releasable P (PRP) was the largest, followed by algal available P (AAP), NaHCO₃ extractable P (Olsen-P), water soluble P (WSP), and readily desorbable P. PRP contributed approximately 60% to total P (TP) in most sediments, AAP 20%, Olsen-P 15%, WSP 2%, and readily desorbable P (RDP) 0.5%. For the heavily polluted sediments, their bioavailable P extracted from TP mainly originated from inorganic P (IP), IP mainly originated from NaOH–P, the bioavailable P concentrations can be evaluated by measuring the concentrations of TP, NaOH–P, and IP. For the slightly polluted sediments, the bioavailable P can only be evaluated by different chemical extractable methods.     

Alpine lake sediment records of the impact of glaciation and climate change on the biogeochemical cycling of soil nutrients

Lake sediment cores from the Coast Mountains of British Columbia were analyzed using chemical sequential extractions to partition the dominant geochemical fractions of phosphorus (P). The P fractions include mineral P (the original source of bioavailable P), occluded P (bound to soil oxides), and organic P (remains of organic matter). By comparing P fractions of soil and recent lake sediment samples, these fractions are shown to be a valid proxy for landscape-scale nutrient status. Changes in soil development for an alpine watershed (Lower Joffre Lake) are inferred from the P fractions in the basin's outlet lake sediments. Glacially sourced mineral P dominates at the base of the core, but several rapid shifts in P geochemistry are evident in the first ∼3000 yr of the record. The latter indicates an interval of early and rapid soil nutrient maturation from ∼9600 to 8500 cal yr BP and a significant influx of slope-derived material into Lower Joffre Lake. A substantial increase in mineral P occurs at ca. 8200 cal yr BP, consistent with the cold event in the vicinity of the North Atlantic at that time. The more recent record reveals a continual increase in the proportion of mineral P from glacial sources to the lake, indicating a trend toward cooler conditions in the Coast Mountains.     

太湖入湖河道沉积物中生物利用磷和营养水平分析

为了解太湖入湖河道的营养状况,研究了太湖西部河流沉积物生物利用磷的组成与分布。研究结果显示,北部沉积物中营养元素较高,南部较低;沉积物中生物利用磷的含量次序为藻类可利用磷(AAP)>NaHCO3提取磷(OLP)>水溶性磷(WSP)>易解吸磷(RDP),其中AAP是重要的生物利用磷,AAP的比例越高,富营养化程度越高。AAP与营养元素的相关性在不同区域河道有所不同,北部河道与总氮(TN)、总磷(TP)相关性较好,中部和南部河道与沉积物有机质总量(TOM)相关性较好。沉积物的生物利用磷受不同污染源影响较大。对比河道沉积物与湖泊沉积物的特征,发现湖泊沉积物中生物利用磷(BAP)/总磷(TP)、藻类可利用磷(AAP)/总磷(TP)都高于河道沉积物,表明湖泊沉积物中的磷更容易被植物吸收。     

Seasonal and spatial changes in water and sediment quality variables in Bafa Lake

The brackish Bafa Lake located in the southwestern part of Turkey is under stress because of both natural and untreated wastewater effluents. The purpose of this research is to determine spatiotemporal distributions of some physicochemical variables in water column (temperature, salinity, pH, conductivity, dissolved oxygen, NH₄–N, NO₂–N, NO₃–N, oPO₄–P, TPO₄–P, chlorophyll-a, total suspended solids) and sediment (TN, TC, TOC, TP) and their relationships at coastal stations. In the water column, nitrate and phosphate concentrations showed seasonal variations with high values recorded in winter period. Ammonium was determined as a main source of TIN component. During summer period, a large amount of total phosphorus was found as dissolved organic form. However, in the winter period, inorganic phosphate levels increased at sampling stations. N limitation was a common feature throughout the lake where P-limitation was only observed in summer period. The total phosphorus levels which showed hypereutrophic condition at the western part of the lake changed between 1.55 and 4.99 μM and did not remain in the range for uncontaminated condition. In the lake sediment, a strong relationship was found between TOC and TC levels. Generally, the mean TOC concentrations constitute small amount of TC values in the sampling stations. The results also indicated that a strong correlation exists between TOC and TN values, and TN was greatly regulated by organic sources. In the lake, TOC:TN ratios changed between 5 and 13; the ratio greater than 10 could be an indicator of algal and land plant sources mixing as an organic matter.     

Weathering of phosphorus-bearing mineral powder and calcium phosphate by Aspergillus niger

The weathering of phosphorus-bearing mineral powder(PBMP) and calcium phosphate(CP) by Aspergillus niger was compared,and the mechanism involved was analyzed for the comprehensive utilization of PBMP.The concentration of water-soluble phosphorus(WSP),Mg2+,and Ca2+at different culture times,microstructures of particles,and mineral compositions was examined by ultraviolet-visible spectrometer(UV),atomic absorption spectrometry(AAS),scanning electron microscopy(SEM),and X-ray diffraction(XRD).Results showed that the change in the concentrations of WSP,Mg2+,and Ca2+were related to the growth of A.niger and the different mineral compositions.Compared with CP,PBMP was weathered harder by fungi.Traces of the weathered mineral were found through SEM.CP not only showed traces of erosion damage but also appeared as a rhombohedron-like substance.The XRD test indicated that the weathering minerals can form water calcium oxalate.Further analysis revealed that the mechanism of PBMP and CP weathering by A.niger was the collaborative result of mycelium biomechanical effects and the acid-soluble role of acidic metabolites.The phosphorus dissolution rate of PBMP after 20 d was 46.83%,whereas that of CP after 12 d was 91.01%.The findings of this study are significant to the effective use of waste PBMP and to the exploitation of low-grade phosphate rock resources.     

Seasonal variations of phosphorus species in sediment from the middle Adriatic Sea

Phosphorus (P) species concentrations in 0–2 cm surface sediment layer were investigated monthly from November 2001 to December 2002 at the bay, channel and open sea stations in the middle Adriatic. Modified SEDEX method was used for inorganic phosphorus species determination [P in biogenic (P-FD), authigenic (P-AUT), detrital apatite (P-DET) and P adsorbed on to iron oxides and hydroxides (P–Fe)], and organic phosphorus (P-ORG). P-FD, P-AUT and P-DET concentration ranges (1.5–5.4, 0–2.7 and 0.4–3.4 μmol g⁻¹, respectively) were similar at all stations, and showed no obvious common trend of seasonal changes. P–Fe ranged from 1.9 to 11.9 μmol g⁻¹ with the highest values at bay station and higher seasonal oscillations than other inorganic P forms. P-ORG ranged from 0.3 to 18.7 μmol g⁻¹ with higher concentrations at stations of fine-sized sediments and showed increased concentrations in warm part of the year at all stations. Correlation between concentrations of P–Fe in the surface sediment layer and orthophosphate sediment-water interface concentration gradients at bay and channel stations indicated to P–Fe importance in the orthophosphate benthic flux. For the bay station, linkage between sediment P-ORG and chlorophyll a concentrations, primary production and microzooplankton abundance was established, indicating a 1 month delay of sediment response to production fluctuations in the water column.     

Importance of terrestrially-derived,particulate phosphorus to phosphorus dynamics in a west coast estuary

Allochthonous inputs of suspended particulate matter from freshwater environments to estuaries influence nutrient cycling and ecosystem metabolism. Contributions of different biogeochemical reactions to phosphorus dynamics in Tomales Bay, California, were determined by measuring dissolved inorganic phosphorus exchange between water and suspended particulate matter in response to changes in salinity, pH, and sediment redox. In serum bottle incubations of suspended particulate matter collected from the major tributary to the bay, dissolved inorganic phosphorus release increased with salinity during the initial 8 h; between 1–3 d, however, rates of release were similar among treatments of 0 psu, 16 psu, 24 psu, and 32 psu. Release was variable over the pH range 4–8.5, but dissolved inorganic phosphorus releases from sediments incubated for 24 h at the pH of fresh water (7.3) and seawater (8.1) were similarly small. Under oxidizing conditions, dissolved inorganic phosphorus release was small or dissolved inorganic phosphorus was taken up by particulate matter with total P content <50 μmoles P g^?1; release was greater from suspended particulate matter with total phosphorus content >50 μmoles P g^?1. In contrast, under reducing conditions maintained by addition of free sulfide (HS^?), dissolved inorganic phosphorus was released from particles at all concentrations of total phosphorus in suspended particulate matter, presumably from the reduction of iron oxides. Since extrapolated dissolved inorganic phosphorus release from this abiotic source can account for only 12.5% of the total dissolved inorganic phosphorus flux from Tomales Bay sediments, we conclude most release from particles is due to organic matter oxidation that occurs after estuarine deposition. The abiotic, sedimentary flux of dissolved inorganic phosphorus, however, could contribute up to 30% of the observed net export of dissolved inorganic phosphorus from the entire estuary.     

Flotation of calcareous Mussorie phosphate ore

Separation of Mussorie rock phosphate (P₂O₅ = 20%) from Uttar Pradesh, India, containing pyrite, calcite and other carbonaceous impurities by flotation has been successfully attempted to upgrade the phosphate values. Based on Hallimond cell flotation results of single and synthetic mineral mixtures of calcite and apatite using oleic acid and potassium phosphate, conditions were obtained for the separation of calcite from apatite which is considered to be the most difficult step in the beneficiation of calcareous phosphates. Further studies using 250 g of the mineral (?60 +150 and ?150 mesh fractions, deslimed) in laboratory size Fagergren subaeration machine employed a stagewise flotation viz. carbonaceous materials using terpineol, pyrite using potassium-ethyl xanthate and calcite using oleic acid respectively. Separation was, however, found to be unsatisfactory in the absence of a depressant.Among starch, hydrofluosilicic acid and dipotassium hydrogen phosphate, which were tried as depressants for apatite in the final flotation stage, dipotassium hydrogen phosphate proved to be superior to others. However, the tests with the above fractions did not yield the required grade. This was possibly due to insufficient liberation of the phosphate mineral from the ore body and different experimental conditions due to scale up operations. Experiments conducted using ?200 mesh deslimed fractions has yielded an acceptable grade of 27.6% P₂O₅ with a recovery of about 60%. The results have been explained in terms of the specific adsorption characteristics of phosphate ions on apatite and the liberation size of the mineral.     

Chemical speciation of fine particle bound trace metals

This study reported quantifications of fine particle bound trace metals and their potential health risks for residents in Guangzhou, a rapidly developing and most populated city in South China. The fine particle samples were collected from October 29^th. to November 8^th. of 2006 at two different elevations in a mainly residential area and analyzed for the total concentration of aluminum, iron, zinc, lead, manganese, copper, arsenic, chromium, nickel, cadmium, molybdenum and cobalt. Results showed that the fine particle concentrations ranged from 95.8μg/m³to 194.7 μg/m³ at the ground and 83.3-190.0 μg/m³ on the roof, which were much higher than the 24 h fine particle standard (35 μg/m³) recommended by USEPA. The total concentrations of zinc, lead, arsenic, chromium and cadmium in fine particle were 504.8, 201.6, 24.3, 7.7 and 4.4 ng/m³, respectively, which were comparable to other major cities of China, but much higher than major cities outside of China. A sequential extraction procedure was used to fractionate these fine particle bound metals into four different fractions. Results indicated that most toxic metals were mainly distributed in bioavailable fractions. For instance, about 91 % of cadmium, 85 % of lead and 74 % of arsenic were in bioavailable forms. Risk calculations with a simple exposure assessment model showed that the cancer risks of the bioavailable fractions of arsenic, chromium and cadmium were 3 to 33 times greater than usual goal, indicating serious health risks to the residents in this urban area.     

The influence of three mangrove species on the distribution of inorganic nitrogen and phosphorus in the Quanzhou Bay estuarine wetland soils

This study aims to investigate the effects of region and three regional dominated mangrove species (Avicennia marina, Aegiceras corniculatum and Kandelia candel) on the distribution of inorganic nitrogen and phosphorus. Measurement of the inorganic nitrogen and phosphorus and enzymatic activities was carried out in soils covered by three mangrove species in the Quanzhou Bay estuarine wetlands, a typical coastal wetland in China. Species with a higher biomass in upstream and midstream absorb more nitrogen from soils, and the retention of the available phosphorus in the soils of different regions causes the regional variation of phosphorus. In areas dominated by A. marina, nitrate nitrogen is lower while available phosphorus is higher. Meanwhile, nitrate nitrogen and available phosphorus are higher in the soils covered by K. candel. Moreover, all three species affect the elemental and enzymic stoichiometry. The mangrove species influences the diversity of the elemental and enzymic stoichiometric relationship through differential microenvironments, which induce the biodiversity of wetland ecosystems. Thus, this study may facilitate a better understanding of the transformation ability of mangroves to nitrogen and phosphorus and will therefore be beneficial for providing a basis for the ecological restoration of estuarine wetlands.     

Spatial variations and distributions of phosphorus and nitrogen in bottom sediments from a typical north-temperate lake,China

Concentrations and vertical distributions of total nitrogen (TN), total phosphorus (TP) and their different forms in sediments obtained from nine locations of Lake Dalinouer in September 2008 were analyzed. The results demonstrated that TP in surface sediments ranged from 0.493 to 0.904 g/kg, and inorganic phosphorus was the main fraction of total phosphorus, ranging from 335 to 738 mg/kg. Simultaneously, the autogenetic calcium phosphorus (ACa-P) was the main fraction of inorganic phosphorus, ranging from 145.4 to 543.2 mg/kg. Vertical distribution of different phosphorus forms in different sediment cores was distinguishing, and most of them tended to increase toward the surface sediment, indicated that the phosphorus concentration was related to the humanity with a certain extent. The relationships between TP and occluded phosphorus and ACa-P were significant. Nitrogen in the sediment was composed mainly of organic nitrogen, accounting for grater than 80 % of TN. NO₃ ^?-N was the dominate fraction of inorganic nitrogen in the surface sediment, ranging between 51 and 346 mg/kg (151.1 ± 104.4 mg/kg), and accounting for between 2.2 and 17.7 % of total sediment nitrogen (6.2 ± 5.6 %). The ratio of organic carbon and TN in sediment was in range of 6.0–25.8 and presented a tendency of lake centre >lake sides, indicating that nitrogen accumulated in the sediments from lake sides came mainly from terrestrial source and nitrogen was mainly autogenetic in lake centre. Ratio of N:P in all sampling sites was below 14, indicated that N was the limiting nutrient for algal growth in this lake.     

Nature and geochemistry of surface sediments of the mangrove environment along the Egyptian Red Sea coast

Grain size and geochemical analyses have been carried out on 58 samples collected from different areas of mangrove environment of the Egyptian Red Sea coast. The texture characteristics of mangrove sediments show that the mean size decreases in sediments of coastal areas while increase in island sediments and the sediment type generally changes from sand to slightly gravelly muddy sand. The sediments are composed mainly of poorly sorted, negatively nearly symmetrical and leptokurtic fine sands. Cluster analysis showed that, distribution of gravel, sand and mud fractions is related to bottom facies and type of sediment source. Generally, sand fraction is the main category among the three constituents. Geochemically the factor controlling the carbonate content of studied sediments includes material supply of biogenic and terrigenous components. Therefore, sediments of Hamata area, km 17 south Safaga, Wadi El-Gemal Island and Abu-Minqar Island are terrigenous sediments, while sediments of km 37 north Quseir are highly carbonates. In general organic matter is higher in the mangrove sediments relative to adjacent areas. The high organic matter in the mangrove sediments is primarily due to the high supply from primary productivity, terrestrial and reworked sediments. Texture is the main controlling factor for the organic matter enrichment. Spatial variations in the phosphorus content in the different studied localities are related to the sources of phosphorus to the area. In comparison, cluster analysis indicates that phosphorus might be transported from terrestrial source to the sea through wadis draining the excavated Upper Cretaceous phosphate rocks. Also, the abundance of phosphorus content may be attributed to phosphatization of calcareous skeletons. Our observations provide knowledge on the physico-chemical effects and will be useful in the management and suitable development of the areas under study. In addition it represent database in the future.     

Abundance and Chemical Speciation of Phosphorus in Sediments of the Mackenzie River Delta, the Chukchi Sea and the Bering Sea: Importance of Detrital Apatite

Utilizing a sequential extraction technique this study provides the first quantitative analysis on the abundance of sedimentary phosphorus and its partitioning between chemically distinguishable phases in sediments of the Bering Sea, the Chukchi Sea and the Mackenzie River Delta in the western Arctic Ocean. Total sedimentary phosphorus (TSP) was fractionated into five operationally defined phases: (1) adsorbed inorganic and exchangeable organic phosphorus, (2) Fe-bound inorganic phosphorus, (3) authigenic carbonate fluorapatite, biogenic apatite and calcium carbonate-bound inorganic and organic phosphorus, (4) detrital apatite, and (5) refractory organic phosphorus. TSP concentrations in surface sediments increased from the Chukchi Sea (18 μmol g⁻¹ of dried sediments) to the Bering Sea (22 μmol g⁻¹) and to the Mackenzie River Delta (29 μmol g⁻¹). Among the five pools, detrital apatite phosphorus of igneous or metamorphic origin represents the largest fraction (~43%) of TSP. The second largest pool is the authigenic carbonate fluorapatite, biogenic apatite as well as CaCO₃ associated phosphorus (~24% of TSP), followed by the Fe-bound inorganic phosphorus, representing ~20% of TSP. The refractory organic P accounts for ~10% of TSP and the readily exchangeable adsorbed P accounts for only 3.5% of TSP. Inorganic phosphorus dominates all of phosphorus pools, accounting for an average of 87% of the TSP. Relatively high sedimentary organic carbon and total nitrogen contents and low δ¹³C values in the Mackenzie River Delta together with the dominance of detrital apatite in the TSP demonstrate the importance of riverine inputs in governing the abundance and speciation of sedimentary phosphorus in the Arctic coastal sediments.