The chemical character and behaviour of phosphorus in poorly oxygenated sediments from open sea to organic-rich inner bay in the Baltic Sea

The chemical composition and vertical distribution of phosphorus (P) in poorly oxygenated sediments in a continuum extending from the open Baltic Sea towards an organic-rich inner bay were characterized by sequential extraction to examine the potential for release of sediment P. The chemical composition of P was related to chemical and physical characteristics of the sediments and the chemistry of pore water and near-bottom water to better understand the behaviour of P. Sediment P increased towards the inner bay, and the concentration of organic matter appeared to dictate its composition: the dominance of apatite-P turned to dominance of organic P (OP). Sediment P burial and, thus, release from sediment P reserves varied depending on the chemical composition of P. Dissolved species at the sediment–water interface suggested fluctuating redox conditions that affect P binding at short time scale. Redox-sensitive, iron (Fe)-bound P was usually relatively low because of poor oxygen (O₂) conditions, which emphasized the role of OP in P release. The results indicate that, over the long term, the abundant organic P reserve may support a significant continuing P release from hypoxic sediments in the severely eutrophied Gulf of Finland (GoF) because capture of P into Fe oxyhydroxides at the sediment surface is restricted. The average long-term minimum annual rate of P release from poorly oxygenated sediments below about 60 m depth in the GoF was approximated on the basis of the vertical distribution of sedimentary P forms and estimates of sedimentation rate.     

Dissolved iron:phosphate ratio as an indicator of phosphate release to oxic water of the inner and outer coastal Baltic Sea

Pore water concentrations and benthic fluxes of dissolved Fe, P and N were measured at two coastal basins in the Gulf of Finland, northern Baltic Sea, during a seasonal cycle. The bioturbated inner coastal basin, where exchange of near-bottom water is efficient, had a better ability to retain P in sediments than the outer basin, where near-bottom water O₂ concentration decreases during summer. Under the presence of O₂ high pore water dissolved Fe:P ratio (>3.6 w:w) in surface layer of the sediment, measured especially in winter, indicated negligible or low P-release and high N:P ratio in the efflux. On the contrary, low Fe:P ratio (<3.6), measured in summer and autumn, indicated high efflux of P and low N:P flux ratio. The low dissolved Fe:P ratio suggested that there was not enough diffusing Fe to form Fe³⁺ oxide-rich layer in the oxic surface zone of the sediments or near-bottom water to bind the P diffusing from the sediment. However, in sediments bioturbated by the abundant bivalve Macoma baltica, small efflux of P were measured almost throughout the study period. Thus, the Fe:P ratio cannot alone explain the P-release in bioturbated sediments. The low N:P ratio in the efflux measured in summer and autumn partly explains the measured low N:P ratio in the near-bottom water and thus N limitation of primary production in the Gulf. Additionally, it is evident that the release of P in the Gulf itself is of great importance for the trophic state of the Gulf of Finland.     

Abundance and activity of microorganisms at the water-sediment interface and their effect on the carbon isotopic composition of suspended organic matter and sediments of the Kara Sea

At ten stations of the meridian profile in the eastern Kara Sea from the Yenisei estuary through the shallow shelf and further through the St. Anna trough, total microbial numbers (TMN) determined by direct counting, total activity of the microbial community determined by dark CO₂ assimilation (DCA), and the carbon isotopic composition of organic matter in suspension and upper sediment horizons (δ¹³C, ‰) were investigated. Three horizons were studied in detail: (1) the near-bottom water layer (20–30 cm above the sediment); (2) the uppermost, strongly hydrated sediment horizon, further termed fluffy layer (5–10 mm); and (3) the upper sediment horizon (1–5 cm). Due to a decrease in the amount of isotopically light carbon of terrigenous origin with increasing distance from the Yenisei estuary, the TMN and DCA values decreased, and the δ¹³C changed gradually from ?29.7 to ?23.9‰. At most stations, a noticeable decrease in TMN and DCA values with depth was observed in the water column, while the carbon isotopic composition of suspended organic matter did not change significantly. Considerable changes of all parameters were detected in the interface zone: TMN and DCA increased in the sediments compared to their values in near-bottom water, while the 13C content increased significantly, with δ¹³C of organic matter in the sediments being at some stations 3.5–4.0‰ higher than in the near-bottom water. Due to insufficient illumination in the near-bottom zone, newly formed isotopically heavy organic matter (δ¹³C ～ ?20‰) could not be formed by photosynthesis; active growth of chemoautotrophic microorganisms in this zone is suggested, which may use reduced sulfur, nitrogen, and carbon compounds diffusing from anaerobic sediments. High DCA values for the interface zone samples confirm this hypothesis. Moreover, neutrophilic sulfur-oxidizing bacteria were retrieved from the samples of this zone.     

Vertical distribution and chemical character of sediment phosphorus in two shallow estuaries in the Baltic Sea

The vertical distribution of various phosphorus (P) forms and their relation to physico-chemical properties of estuary sediment material were studied to better understand the potential release and burial of P. Core samples were taken from two dissimilar estuaries in the Baltic Sea: one in the Archipelago Sea (AS) and one in the Gulf of Finland (GoF). The P reserves were characterized by a sequential extraction procedure including the analysis of simultaneously dissolved elements in two extraction steps. The sediment material was also analysed for particle size distribution and total elements. In addition, several environmental variables were determined. The occurrence of the various forms of P varied with sediment depth among different sites. Reductant soluble, iron (Fe) bound P was the most dynamically changing P form in the sediment, while P bound to other metal oxides and apatite-P were the most stable fractions. High sedimentation rate was a dominating factor for sediment P burial. In addition, the content of organic matter, the amount of erosion-transported sorption components, and the oxygen (O₂) conditions in the near-bottom water were important determinants of the behaviour of sediment P. The results indicate that, over the long term, both estuaries have acted as sinks for deposited P and restricted the transport of P to the AS and the open GoF, thereby partly alleviating the eutrophication process.     

Carbon isotopic composition in suspended organic matter and bottom sediments of the East Arctic seas

The samples of water and bottom sediments of the East Siberian and Chukchi Seas collected during the second Russian-American RUSALCA expedition were used to analyze patterns of the isotopic composition of carbon in the organic matter (OM) of suspended material (SOM) and bottom sediments (BOM). Similar to other marine environments, the SOM isotopic composition depended on the ratio between the terrigenous and planktonic OM, both in the water body as a whole and in its parts. Thus, in the East Siberian Sea the carbon of SOM was poorer in ¹³C (??¹³C = ?24.51??) than the open part of the more productive Chukchi Sea (??¹³C = ?22.16??). In the less productive coastal waters of the Chukchi Sea, the ratio of terrigenous OM increased, resulting in a ??¹³C shift to lower values (?23.40??). Due to the influx of reduced products of anaerobic diagenesis of the sediments, elevated total number of microorganisms and dark CO₂ fixation were found in the near-bottom water at the water-sediment biogeochemical barrier. The newly formed biomass of autotrophic microorganisms shifted the carbon isotopic composition of the near-bottom suspended material to more positive ??¹³C values, with the average values of ?23.39 and ?20.37?? for the East Siberian and Chukchi Sea, respectively. Changes in the carbon isotopic composition of OM resulting from microbial activity continued in the upper sediment layers. When the rate of biomass synthesis increased that of biomass consumption, the ¹³C content increased further. At higher rates of OM mineralization, ¹²C accumulated in its remaining part.     

Coupled Dynamics of Iron and Phosphorus in Sediments of an Oligotrophic Coastal Basin and the Impact of Anaerobic Oxidation of Methane

Studies of phosphorus (P) dynamics in surface sediments of lakes and coastal seas typically emphasize the role of coupled iron (Fe), sulfur (S) and P cycling for sediment P burial and release. Here, we show that anaerobic oxidation of methane (AOM) also may impact sediment P cycling in such systems. Using porewater and sediment profiles for sites in an oligotrophic coastal basin (Bothnian Sea), we provide evidence for the formation of Fe-bound P (possibly vivianite; Fe₃(PO₄)₂ ^.8H₂O) below the zone of AOM with sulfate. Here, dissolved Fe²⁺ released from oxides is no longer scavenged by sulfide and high concentrations of both dissolved Fe²⁺ (>1 mM) and PO₄ in the porewater allow supersaturation with respect to vivianite to be reached. Besides formation of Fe(II)-P, preservation of Fe-oxide bound P likely also contributes to permanent burial of P in Bothnian Sea sediments. Preliminary budget calculations suggest that the burial of Fe-bound P allows these sediments to act as a major sink for P from the adjacent eutrophic Baltic Proper.     

Phosphorus dynamics in shallow eutrophic lakes: an example from Zeekoevlei,South Africa

Zeekoevlei is the largest freshwater lake in South Africa and has been suffering from hyper-eutrophic conditions since last few decades. We have used total P (TP), dissolved phosphate (PO₄ ³⁻), organic P (OP), calcium (Ca) and iron (Fe) bound P fractions to investigate the relevant physical, chemical and biological processes responsible for sedimentation and retention of P and to study phosphorus (P) dynamics in this shallow lake. In addition, redox proxies (V/Cr and Th/U ratios) are used to study the prevailing redox conditions in sediments. Adsorption by CaCO₃ and planktonic assimilation of P are found to control P sedimentation in Zeekoevlei. Low concentration of the labile OP fraction in surface sediments restricts the release of P by bacterial remineralisation. Low molar Ca/P and Fe/P ratios indicate low P retention capacity of sediments, and P is most likely released by desorption from wind-induced resuspended sediments and mixing of pore water with the overlying water column. Handling editor: J. Saros     

Organic matter composition in coastal sediments at Terra Nova Bay (Ross Sea) during summer 1995

We illustrate the spatial and vertical distribution of sediment phytopigments and organic matter biochemical composition at Terra Nova Bay (Ross Sea) during summer 1995. Coastal sediments displayed high phytopigments concentrations associated with huge amounts of labile organic matter largely dominated by proteins. This result was opposite to previous observations in the same area. Such comparison suggested that whilst organic matter quantity in the sediments depended upon the vertical input from the water column, temporal changes in its biochemical composition were related to benthic processes. As considerably high concentrations of biopolymeric organic carbon were found even at 6-cm depth and according to the “loss type” functioning of the coastal waters of the Ross Sea, we stress the summer time occurrence in coastal sediments of an important organic matter burial. Accepted: 24 October 1999     

Microbiological and biogeochemical processes in a pockmark of the Gdansk depression,Baltic Sea

Comprehensive microbiological and biogeochemical investigation of a pockmark within one of the sites of gas-saturated sediments in the Gdansk depression, Baltic Sea was carried out during the 87th voyage of the Professor Shtokman research vessel. Methane content in the near-bottom water and in the underlying sediments indicates stable methane flow from the sediment into the water. In the 10-m water layer above the pockmark, apart from methane anomalies, elevated numbers of microorganisms and enhanced rates of dark CO₂ fixation (up to 1.15 µmol C/(l day)) and methane oxidation (up to 2.14 nmol CH₄/(l day)) were revealed. Lightened isotopic composition of suspended organic matter also indicates high activity of the near-bottom microbial community. Compared to the background stations, methane content in pockmark sediments increased sharply from the surface to 40–60 ml/dm³ in the 20–30 cm horizon. High rates of bacterial sulfate reduction (SR) were detected throughout the core (0–40 cm); the maximum of 74 µmol S/(dm³ day) was located in subsurface horizons (15–20 cm). The highest rates of anaerobic methane oxidation (AMO), up to 80 µmol/dm³ day), were detected in the same horizon. Good coincidence of the AMO and SR profiles with stoichiometry close to 1: 1 is evidence in favor of a close relation between these processes performed by a consortium of methanotrophic archaea and sulfate-reducing bacteria. Methane isotopic composition in subsurface sediments of the pockmark (from ?53.0 to ?56.5‰) does not rule out the presence of methane other than the biogenic methane from the deep horizons of the sedimentary cover.     

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.     

Links between Geographic Location, Environmental Factors, and Microbial Community Composition in Sediments of the Eastern Mediterranean Sea

The bacterial community composition of marine surface sediments originating from various regions of the Eastern Mediterranean Sea (12 sampling sites) was compared by parallel use of three fingerprinting methods: analysis of 16S rRNA gene fragment heterogeneity by denaturing gradient electrophoresis (DGGE), terminal restriction fragment length polymorphism (T-RFLP), and analysis of phospholipid-linked fatty acid composition (PLFA). Sampling sites were located at variable depths (30–2860 m; water column depth above the sediments) and the sediments differed greatly also in their degree of petroleum contamination (0.4–18 μg g⁻¹), organic carbon (0.38–1.5%), and chlorophyll a content (0.01–7.7 μg g⁻¹). Despite a high degree of correlation between the three different community fingerprint methods, some major differences were observed. DGGE banding patterns showed a significant separation of sediment communities from the northern, more productive waters of the Thermaikos Gulf and the oligotrophic waters of the Cretan, S. Ionian, and Levantine Sea. T-RFLP analysis clearly separated the communities of deep sediments (>1494 m depth) from their shallow (<617 m) counterparts. PLFA analysis grouped a shallow station from the productive waters of the north with the deep oligotrophic sediments from the Ionian and Levantine Sea, with low concentrations of PLFAs, and hence low microbial biomass, as the common denominator. The degree of petroleum contamination was not significantly correlated to the apparent composition of the microbial communities for any of the three methods, whereas organic carbon content and sediment chlorophyll a were important in this regard.     

Sulfate reduction, methanogenesis, and methane oxidation in the upper sediments of the Vistula and Curonian Lagoons, Baltic Sea

Microbiological, biogeochemical, and isotope geochemical investigations of the upper sediments of the Vistula and Curonian lagoons, Baltic Sea, were carried out. High content of organic matter in the sediments was responsible for the high numbers (over 10¹⁰ cells cm^?3) and activity of heterotrophic microorganisms. The calculated integral rates of dark CO₂ assimilation for the upper 30 cm of the sediments varied 12.5 to 38.8 mmol m^?2 day^?1 and were somewhat higher in the Curonian Lagoon than in the Vistula Lagoon. Integral rates of sulfate reduction were higher in the more saline Vistula Lagoon. Rapid consumption of sulfates of the pore water resulted in intensified methanogenesis, with significantly higher rates detected in the silts of the Curonian Lagoon. High rates of methanogenesis in the Curonian Lagoon correlated with higher methane levels in its upper sediments and near-bottom water. The highest rates of methane oxidation were detected in the uppermost sediment horizons (oxidized or slightly reduced), which was an indication of the barrier role of aerobic methanotrophic bacteria. The calculated methane flows from the sediments into the water column were 0.45 and 0.007 mmol m^?2 day^?1 for the Vistula and Curonian Lagoons, respectively. Low methane flow from the sediments of the Curonian Lagoon resulted probably from the specific weather (wind) conditions during sampling. The near-stormy conditions in the Curonian Lagoon caused sediment detachment, resulting in methane release into the water column.     

Sediment phosphorus release in phytoplankton dominated versus macrophyte dominated shallow lakes: importance of oxygen conditions

Increased discharges of organic matter from different sources in Morales Stream, one of the main tributaries of the Matanza-Riachuelo River, caused not only an increase in its primary production but also drastic changes in the composition of its sediments, thus favoring eutrophication processes. An in situ study was carried out in order to assess the effects of an organic point source contamination (from intensive cattle rearing) on the sediments of Morales Stream. Surface water and sediment samples were analysed to determine the chemical characteristics of the water–sediment system. The amounts and forms of sediment phosphorus were determined using the `EDTA method' (Golterman, 1996) at two sites of the stream having different nutrient loads. The increase in the organic load of Morales Stream waters influences the dynamics of sediment P, producing two main effects: (1) an increase in the organic matter amount of the sediment that leads to an increase in the amount of P associated to organic fractions, which may be released by bacterial activity under anoxic conditions; and (2) a decrease in the concentration of P in the fraction bound to iron. Morales Stream sediments may act as a potential source of P, which can release this nutrient to water under the reducing conditions originated by uncontrolled discharges of organic residues to this water body.     

Release rates and potential fates of nitrogen and phosphorus from sediments in a eutrophic reservoir

1. Nutrients released from lake sediments can influence water column nutrient concentrations and planktonic productivity. We examined sediment nutrient release [soluble reactive phosphorus (SRP) and ammonia (NH)] at two sites in a eutrophic reservoir (Acton Lake, OH, U.S.A.) that differed in physical mixing conditions (a thermally stratified and an unstratified site). 2. Sediment nutrient release rates were estimated with three methods: sediment core incubations, seasonal in situ hypolimnetic accumulation and a published regression model that predicted sediment phosphorous (P) release rate from sediment P concentration. All three methods were applied to the deeper stratified site in the reservoir; however, we used only sediment core incubations to estimate SRP and NH release rates at the shallow unstratified site because of the lack of thermal stratification. We also compared the total P concentration (TP_S) of sediments and the concentration of P in various sediment fractions at both sites. 3. Anoxic sediments at the stratified site released SRP at rates more than an order of magnitude greater than oxic sediments at the shallow unstratified site. However, P accumulated in the hypolimnion at much lower rates than predicted by sediment core incubations. In contrast, NH was released at similar rates at both sites and accumulated in the hypolimnion at close to the expected rate, indicating that P was ‘lost’ from the hypolimnion through biogeochemical pathways for P, such as precipitation with inorganic material or biological uptake and sedimentation. 4. TP_S was significantly greater at the deeper stratified site and organically bound P accounted for >50% of TP_S at both sites. 5. We examined the magnitude of SRP fluxes into the study reservoir in 1996 by comparing the mean summer daily SRP fluxes from anaerobic sediments, aerobic sediments, stream inflows and gizzard shad excretion. While the SRP release from anaerobic sediments was high, we hypothesise that little of this SRP gained access to the epilimnion in mid‐summer. SRP flux to the reservoir from aerobic sediments was less than from gizzard shad excretion and streams. Large interannual variability in thermocline stability, gizzard shad biomass and stream discharge volumes, will affect SRP loading rates from different sources in different years. Therefore, construction of P budgets for different years should account for interannual variation in these parameters.     

Binding of phosphate in sediment accumulation areas of the eastern Gulf of Finland,Baltic Sea

The relationships between P and components binding P were studied by analysing the concentrations of N, P, Fe, Mn, Ca and Al in sediments and pore water along the estuarine transect of the River Neva in August 1995. The high sediment organic matter concentration resulted in low surface redox potential and high pore-water o-P concentration, whereas the abundance of amphipods resulted in high surface redox potentials and low pore-water o-P concentration. However, despite the variation in sediment organic matter and the abundance of amphipods, very reduced conditions and slightly variable concentrations of Tot-P (0.7–1.1 mg g^–1 DW) were observed in the 10–15 cm sediment depth along the estuarine gradient, indicating that the pools of mobile P were largely depleted within the depth of 0–15 cm. Multiple regression analysis demonstrated that organic matter and Tot-Fe concentration of the sediment were closely related to the variation in Tot-P concentration of the sediments (r ² = 0.817, n=32). In addition, the high total Fe:P ratio suggested that there is enough Fe to bind P in sediments along the estuarine gradient. However, low Fe_diss concentrations in the pore water of reduced sediment (redox-potential <–50 mV) indicated efficient precipitation of FeS (FeS and FeS₂), incapable to efficiently bind P. Consequently, the low Fe_diss:o-P ratio (< 1) recorded in pore water in late summer implied that Fe³⁺ oxides formed by diffusing Fe_diss in the oxic zone of the sediments were insufficient to bind the diffusing o-P completely. The measured high o-P concentrations in the near-bottom water are consistent with this conclusion. However, there was enough Fe_diss in pore water to form Fe³⁺ oxides to bind upwards diffusing P in the oxic sediment layer of the innermost Neva estuary and the areas bioturbated by abundant amphipods.     

Phosphorus Fractionation in Core Sediments from Haihe River Mainstream,China

Sediments from Haihe River mainstream, located in Xingjiaquan, Zhangjiazui, Tianjin, were collected and examined on the basis of P fractionation. SMT (standards, measurements and testing) procedure was adopted to investigate the changes in P concentration with depth in the core sediments collected from the different sampling sites of Haihe River mainstream. The relationships among different P fractions, such as exchangeable P (Ex-P), metal oxide bounded P (NaOH-P), organic matter and grain size, were also discussed. The results indicate that in both sites the rank order of P fractions was HCl-P > Organic P (OP) > NaOH-P > Ex-P in terms of their concentration. The Ex-P represented < 4% of the sediment total P, while the NaOH-P ranged 5–21%. The calcium bound phosphorus (HCl-P) showed considerable contribution (53–80%) to the sediment total P loads. Silt/clay sized sediments exhibited significantly higher concentrations of HCl-P and Ex-P in both sites. However, coarse-sand-sized sediments exhibited significantly higher concentrations of OP in both sites and NaOH-P in Xingjiaquan. Multivariate statistics were performed to identify the factors that influenced the sediment P.     

Extreme water level decline effects sediment distribution and composition in Lake Alexandrina,South Australia

Water level decline affects the biophysical environment of shallow lakes. Unprecedented drought in Australia’s Murray–Darling Basin resulted in extreme water level drawdown in the large, shallow Lake Alexandrina at the end of the River Murray. Surface sediment was collected from 22 sites in the lake before and after water levels declined to assess the integrated limnological changes over the period of drawdown. Results indicate an increase in the proportion of organic particles in profundal sediments, as well as an increase of fine particles (<19.9 μm) in peripheral sediments. These changes to sediment composition corresponded to higher concentrations of suspended particles at low water levels. Increased autochthony and a shift in primary production from macrophytes to phytoplankton in Lake Alexandrina support these findings. Inorganic carbon and other nutrients were lost from sandy sediments most likely through carbonate dissolution driven by a localized decrease in pore water pH from increased mineralisation of organic matter.     

Formation of manganese oxyhydroxides on the Dead Sea coast by alteration of Mn-enriched carbonates

Manganese enriched carbonates preferentially accumulate in near-shore, shallow water sediments of the Dead Sea. These carbonates are formed by coprecipitation of Mn with authigenic aragonite, as well as by direct precipitation of Mn-carbonate from the pore water of the shallow sediments. The primary source of the Mn that accumulates as carbonates is allochthonous Mn-enriched oxides that are eroded from the nearby coasts and become buried within the near-shore shallow water sediments. Due to the decline in the level of the Dead Sea between 1960–1990, bands of sediments (parallel to the current shoreline) which were previously submerged, became exposed to air and consequently desiccated. We suggest that in order to approach new hydraulic equilibrium in some of those coastal areas, the decline in the level of the lake was followed by a lakeward advance of fresher groundwater from the shallow coastal aquifer. Those fresher waters are characterized by a higher pH than the interstitial brine, and therefore a new state of water-rock interaction is established which results in oxidative alteration of Mn-carbonates to Mn-oxides. In addition, manganese-oxidizing bacteria, shown to be active in water with lower salinity than that of the Dead Sea, may also play a part in oxidation of divalent manganese released from the sediment. As a result, some segments of the Dead Sea coast are characterized by black Mn-enriched sediments that in places form crusts over the surface.     

Influence of outbreak of macroalgal blooms on phosphorus release from the sediments in Swan Lake Wetland,China

Macroalgal blooms have occurred worldwide frequently in coastal areas in recent decades, which dramatically modify phosphorus (P) cycle in water column and the sediments. Rongcheng Swan Lake Wetland, a coastal wetland in China, is suffering from extensive macroalgal blooms. In order to verify the influence of macroalgal growth on sediment P release, the sediments and filamentous Chaetomorpha spp. were incubated in the laboratory to investigate the changes of water quality parameters, P levels in overlying water, and sediments during the growth period. In addition, algal biomass and tissue P concentration were determined. In general, Chaetomorpha biomasses were much higher in high P treatments than in low P treatments. Compared with algae+low P water treatment, the addition of sediments increased the algal growth rate and P accumulation amount. During the algal growth, water pH increased greatly, which showed significant correlation with algal biomass in treatments with high P (P < 0.05). P fractions in the sediments showed that Fe/Al–P and organic P concentrations declined during the algal growth, and great changes were observed in algae+low P water+sediment treatment for both. As a whole, the sediments can supply P for Chaetomorpha growth when water P level was low, and the probable mechanism was the release of Fe/Al–P at high pH condition induced by intensive Chaetomorpha blooms.     

Arctic sediments (Svalbard): pore water and solid phase distributions of C,N, P and Si

Pore water and solid phase distributions of C, N, P and Si in sediments of the Arctic Ocean (Svalbard area) have been investigated. Concentrations of organic carbon (C_org) in the solid phase of the sediment varied from 1.3 to 2.8% (mean 1.9%), with highest concentrations found at shallow stations south/southwest of Svalbard. Relatively low concentrations were obtained at the deeper stations north/northeast of Svalbard. Atomic carbon to nitrogen ratios in the surface sediment ranged from below 8 to above 10. For some stations, high C/N ratios together with high concentrations of C_org suggest that sedimentary organic matter is mainly of terrigenous origin and not from overall biological activity in the water column. Organic matter reactivity (defined as the total sediment oxygen consumption rate normalized to the organic carbon content of the surface sediment) correlated with water depth at all investigated stations. However, the stations could be divided into two separate groups with different reactivity characteristics, representing the two most dominant hydrographic regimes: the region west of Svalbard mainly influenced by the West Spitsbergen Current, and the area east of Svalbard where Arctic polar water set the environmental conditions. Decreasing sediment reactivity with water depth was confirmed by the partitioning between organic and inorganic carbon of the surface sediment. The ratio between organic and inorganic carbon at the sediment-water interface decreased exponentially with water depth: from indefinite values at shallow stations in the central Barents Sea, to approximately 1 at deep stations north of Svalbard. At stations east of Svalbard there was an inverse linear correlation between the organic matter reactivity (as defined above) and concentration of dissolved organic carbon (DOC) in the pore water. The more reactive the sediment, the less DOC existed in the pore water and the more total carbonate (C_t or ΣCO₂) was present. This observation suggests that DOC produced in reactive sediments is easily metabolizable to CO₂. Sediment accumulation rates of opaline silica ranged from 0.35 to 5.7 μmol SiO₂ m⁻²d⁻¹ (mean 1.3 μmol SiO₂ m⁻²d⁻¹), i.e. almost 300 times lower than rates previously reported for the Ross Sea, Antarctica. Concentrations of ammonium and nitrate in the pore water at the sediment-water interface were related to organic matter input and water depth. In shallow regions with highly reactive organic matter, a pool of ammonium was present in the pore water, while nitrate conoentrations were low. In areas where less reactive organic matter was deposited at the sediment surface, the deeper zone of nitrification caused a build-up of nitrate in the pore water while ammonium was almost depleted. Nitrate penetrated from 1.8 to ≥ 5.8 cm into the investigated sediments. Significantly higher concentrations of “total” dissolved nitrogen (defined as the sum of NO₃, NO₂, NH₄ and urea) in sediment pore water were found west compared to east of Svalbard. The differences in organic matter reactivity, as well as in pore water distribution patterns of “total” dissolved nitrogen between the two areas, probably reflect hydrographic factors (such as ice coverage and production/import of particulate organic material) related to the dominant water mass (Atlantic or Arctic Polar) in each of the two areas. The data presented were collected during the European “Polarstern” Study (Arctic EPOS) sponsored by the European Science Foundation