Seasonal variation regulate the endogenous phosphorus release in sediments of Shijiuhu Lake via water-level fluctuation.

Freshwater lakes undergo substantial alterations of the phosphorus (P) cycle in the water-sediment ecosystem due to thermal change. The impact process of seasonal fluctuation on P cycling in sediments has been scarcely investigated. P forms in sediments from a freshwater lake in China were analyzed using sequential extraction technique. The vertical distribution of soluble reactive P (SRP), Fe2+, and S2- in the interstitial water was measured using diffusion gradient technique (DGT). Fick's Law and DIFS model were used to obtain the diffusion fluxes of SRP and the kinetic parameters in the water-sediment system. The results showed that total P (TP) concentrations in the solid sediments varied from 207.5, 266.6 and 130.3 mg/kg to 614.7, 1053.1, and 687.6 mg/kg in winter, spring, and summer, respectively. The concentrations of individual P forms in spring were higher than those in other seasons, with Fe-bound P (Fe-P) concentration being the highest across all seasons. Notably, significant variations of SRP concentrations were found in the interstitial water between sedimentary depths of approximately 2 cm and 6 cm, particularly in the summer. Furthermore, higher diffusion fluxes of SRP through the interface were found in summer. A stable anaerobic environment failed to develop in spring with high water level, preventing the desorption of solid Fe-P and diffusion of Fe2+ into the water due to the afflux and deposition of P-containing particulate into deeper sediment layers along with organic material. Under extreme high-temperature in summer, decreased rainfall and rising temperatures boosted the activity of aquatic organisms in the water, thereby reducing P fixation by sediments and leading to P release. This process increased the risk of P excess and potential eutrophication in the water. Generally, clarifying the resupplying processes of endogenous P in sediment systems experiencing seasonal variations is critical for eutrophication management of lakes.

How phoD-harboring functional microbial populations trigger the release risk of phosphorus in water sediment system of Shijiuhu Lake, China after experiencing the transseasonal shift.

Excessive phosphorus (P) enrichment is the critical cause of eutrophication in the lake water. Organic P (Po) mineralization processes induced by alkaline phosphatase (APase) regulated by phoD-encoding microorganisms in the lake ecosystems was still ambiguous due to the transseasonal shift of water temperatures and depths. Different P pools in the water and sediments of Shijiuhu Lake at varied seasons were measured using chemical extraction methods and solution 31P NMR. The alkaline phosphatase activity (APA) in the sediments were assessed together with enzyme kinetic parameters. The abundances and compositions of microbial communities encoding functional gene phoD were also obtained using high-throughput sequencing. The results showed that Po concentrations remarkably increased from winter toward spring when having higher water depths due to the terrigenous input and biomass deposition. Noteworthy elevation in the PO43- concentration was observed in the interstitial water during the spring, particularly at around 5 cm sediment depth with value reaching as high as 0.43 mg/L. The degradation and mineralization of momoesters and diesters with higher concentrations in the sediments of spring aggravated the PO43- load in the interstitial water. Higher APA reaching 91.6 µg/(g·h) in spring was responsible for the mineralization of Po. Remarkably upwards increasing of absolute abundance of phoD-encoding gene in spring reaching up to 2.6 times of that in winter facilitated the generation of APA in spring. Cobetia and Calothrix followed by Aquabacterium and Mitsuaria were the most abundant phoD-encoding genera with relative abundance > 4%. Weakly positive correlation between dominant bacterial genera and APA and P fractions suggested that low-abundance genera was also involved in the APA generation and Po hydrolysis. These results indicate that spring with high water temperature and depth facilitate the mineralization of Po in the sediment and increase of labile PO43- load in the water, further provide valuable information for the management of eutrophic lakes.

Terrestrial sources regulate the endogenous phosphorus load in Taihu Lake, China after exogenous controls: Evidence from a representative lake watershed.

Identifying phosphorus (P) sources and contributions from terrestrial sources is important for clean water and eutrophication management in lake watersheds. However, this remains challenging owing to the high complexity of P transport processes. The concentrations of different P fractions in the soils and sediments from Taihu Lake, a representative freshwater lake watershed, were obtained using sequential extraction procedure. The dissolved phosphate (PO4-P) and alkaline phosphatase activity (APA) in the lake's water were also surveyed. The results showed that different P pools in the soil and sediments displayed different ranges. Higher concentrations of P fractions were measured in the solid soils and sediments from the northern and western regions of the lake watershed, indicating a larger input of P from exogenous sources, including agriculture runoff and industrial effluent from the river. Generally, higher Fe-P and Ca-P concentrations of up to 399.5 and 481.4 mg/kg were detected in soils and lake sediments, respectively. Similarly, the lake's water had higher concentrations of PO4-P and APA in the northern region. A significant positive correlation was found between Fe-P in the soil and PO4-P concentrations in the water. Statistical analysis indicated that appropriately 68.75% P was retained in the sediment from terrigenous sources, and 31.25% P experienced dissolution and shifted to the solution phase in the water-sediment ecosystems. The dissolution and release in Fe-P in the soils were responsible for the increase of Ca-P in the sediment after the afflux of soils into the lake. These findings suggest that soil runoff predominantly controls P occurrence in lake sediments as an exogenous source. Generally, the strategy of reducing terrestrial inputs from agricultural soil discharge is still an important step in P management at the catchment scale of lakes.

Tracing the sources of phosphorus in lake at watershed scale using phosphate oxygen isotope (δ18OP).

Phosphorus (P) is normally considered as the limited nutrient for shallow freshwater lakes and can potentially trigger eutrophication on account of high concentrations. Due to the various transportation and transformation processes, P source apportionment and management in lake ecosystems have become more and more difficult. Combining with sequential extraction of P fractions and mineralogical analysis, the isotopic compositions of oxygen in phosphate (δ18OP) of resin-extractable P from the different samples including soil, estuary sediments, pond sediments, and lake sediments in the Shijiuhu Lake catchment, China, were investigated. The results showed that δ18OP values ranged from +15.23 to +21.92‰ in agricultural soil, +16.53 to +24.10‰ in estuary sediments, +18.90 to +20.90‰ in pond sediments, and +17.42 to +19.70‰ in lake sediments. Isotopic signatures indicated that chemical fertilizers with heavier δ18OP values (+20.70 to +26.50‰) were the predominant contributors of P in the soil. The river transportation together with Fe/Al-P desorption on anaerobic condition simultaneously stimulated the enrichment of P in the lake sediments, even though the biotic activity regulated the isotope values moving toward the equilibrium. Eroded soil was the important source of P in lake and pond sediments via drainage and runoff, and conserved the source isotope signal in the samples. Stronger biotic activity in the aquatic environments dragged δ18OP values toward the equilibrium. However, conspicuous off-equilibrium isotope signature suggested the terrestrial sources in the aquatic ecosystems. The calculation of two end-member linear mixing models suggested that soils also predominantly controlled the P occurrence in the lake sediments with contribution higher than 80%, indicating that decreasing inputs from the agricultural activities is important in P reduction on catchment scale. Generally, δ18OP from different sources can provide indirect and important evidences for the identification and management of P sources in the lake catchment.

Dissimilatory nitrate reduction to ammonium (DNRA) potentially facilitates the accumulation of phosphorus in lake water from sediment.

Nitrogen (N) and phosphorus (P) are crucial nutrients for eutrophication in the lacustrine ecosystem and attract the attention worldwide. However, the interaction between them need further clarification. This study aimed to assess the influence of dissimilatory nitrate reduction to ammonia (DNRA) on the cycle of P in lacustrine sediment. Different fractions of N and P in the pore water were measured using high-resolution in-situ measurement techniques, HR-Peeper and DGT, coupling with sequential extraction for solid sediment from a shallow freshwater lake. The results showed that elevated nitrate (NO3-) reduction via DNRA rather than denitrification was verified at deeper sediment layer, suggesting the generation of inorganic ammonia (NH4+) as electron donor under anaerobic episodes. High abundance of DNRA bacteria (nrfA gene) obtained using high-throughput sequencing analysis were detected at upper layer and responsible for the accumulation of NH4+ in the sediment coupling with chemolithoautotrophic metabolism. Additionally, significant desorption of ionic ferrous iron (Fe2+) and dissolved reactive phosphate (DRP) from solid phase and the enrichment in the solution was simultaneously detected. Higher concentration of solid Fe bound P (Fe-P) at deeper layer indicated the potential re-oxidation of Fe2+ as electron donor during DNRA process and sorption of DRP toward the Fe-containing minerals. However, obvious evidence of desorption proved by DGT indicated that higher NH4+ concentrations favored the reduction of Fe(III) oxy(hydr)oxides and the desorption of DRP into the pore water and diffusion toward the overlying water. Finally, noteworthy S2- release from solid sediment was speculated to stimulate the DNRA and facilitated the accumulation of NH4+ in the solution, which further induced the enrichment of DRP in water from the solid phase. Overall, DNRA potentially facilitates the accumulation of P in lake water, and the synchronous control of N and P is important for the eutrophication management and restoration of lake eutrophication.

How do inundation provoke the release of phosphorus in soil-originated sediment due to nitrogen reduction after reclaiming lake from polder.

Different N and P fractions in microcosm incubation experiment was measured using high-resolution in-situ Peeper and DGT techniques combining with sequential extraction procedure. The results showed the synchronous desorption and release of PO43-, S2- and Fe2+ from the solid soil-originated sediment. This trend indicated that the significant reduction of Fe-P and SO42- occurred in the pore water during the inundation. The concentrations of PO43- in the overlying water and pore water increased to more than 0.1 and 0.2 mg/L at the beginning of the incubation experiment. Decreased NO3-concentrations from more than 1.5 mg/L to less than 0.5 mg/L combining with increasing NH4+ concentrations from less than 1 mg/L to more than 5 mg/L suggested the remarkable NO3- reduction via dissimilatory nitrate reduction to ammonia (DNRA) pathway over time. High NH4+ concentrations in the pore water aggravated the release of Fe2+ through reduction of Fe(III)-P as electric acceptors under anaerobic conditions. This process further stimulated the remarkable releasing of labile PO43- from the solid phase to the solution and potential diffusion into overlying water. Additionally, high S2- concentration at deeper layer indicated the reduction and releasing of S2- from oxidation states, which can stimulated the NO3- reduction and the accumulation of NH4+ in the pore water. This process can also provoke the reduction of Fe-P as electric acceptors following the release of labile PO43- into pore water. Generally, inundation potentially facilitate the desorption of labile P and attention should be paid during the reclaiming lake from polder.

Phosphorus removal from sediments by Potamogeton crispus: New high-resolution in-situ evidence for rhizosphere assimilation and oxidization-induced retention.

Macrophytes are usually chosen for phytoremediation tools to remove P in eutrophic aquatic ecosystems, but the lack of test methods hinders the understanding of removal mechanism and application. In this study, we used the novel technologies combined of Diffusive gradients in thin films (DGT), Planar optode (PO), and Non-invasive micro-test technology (NMT) to explore P dynamics in water-sediment continuum and rhizosphere of Potamogeton crispus over time. Results of the high-resolution in situ measurement showed that labile P(LPDGT) fluxes at the surficial sediment significantly decreased from approximate 120, 140, and 200 pg/ (cm2•sec) via 30 days incubation period to 17, 40, and 56 pg/(cm2•sec) via that of 15 days. Obvious synchronous increase of LPDGT was not detected in overlying water, suggesting the intense assimilation of dissolve reactive P via root over time. PO measurement indicated that O2 concentration around the rhizosphere remarkably increased and radially diffused into deeper sediment until 100% saturation along with the root stretch downwards. NMT detection of roots showed the obvious O2 inflow into root tissue with the uppermost flux of 30 pmol/(cm2•sec) from surroundings via aerenchyma on different treatment conditions. Different from previous reports, gradually saturating O2 concentrations around the rhizosphere was principally driven by O2 penetration through interspace attributing to root stretch downward rather than root O2 leakage. Increased O2 concentrations in deep sediment over time finally induced the oxidization of labile Fe(II) into Fe(III) bound P and local P immobilization.

Tracing the sources of phosphorus along the salinity gradient in a coastal estuary using multi-isotope proxies.

Eutrophication in coastal water has compromised ecosystem services. Identification of phosphorus (P) sources and their load contributions are required for the development of effective nutrient management plans. In this research, multi-isotope proxies were applied to track P sources and evaluate their relative contributions in Love Creek, a coastal estuary in Delaware. The isotope values of carbon (ca. -22‰), nitrogen (ca.+6‰), and phosphate oxygen (ca.+18‰) of agricultural soils under different agricultural practices are generally similar even though their concentrations are distinctly different from forest soils (δ13C: ca. -27‰; δ13N: ca.+2‰; δ18OP: ca.+22‰). Comparison of these parameters among potential land sources (agricultural soils, forest soils, septic wastes, and plant debris) and sink (colloids in water) revealed that the plant debris and soils from forest sources are likely dominant sources of P in freshwater sites. The contribution of terrestrial P sources gradually decreased along the salinity gradient and agricultural soil sources gradually dominanted in the saline water portion of the creek. The variations of P loads due to weather-related discharge, changing land use and activities, and seasons were high and reflected the limitation of accurate estimation of sources. Overall, these results provide improved insights into potential sources and biogeochemical processes in the estuary, which are expected to be useful for water quality monitoring programs.

Water-level fluctuations regulate the availability and diffusion kinetics process of phosphorus at lake water-sediment interface.

Sequential extraction and in-situ diffusive gradients in thin films (DGT) techniques were used to determine phosphorus (P) fractions and high-resolution 2D fluxes of labile PDGT, Fe2+DGT, and S2-DGT in sediment systems. The diffusion fluxes were subsequently calculated for different scenarios. Dynamic diffusion parameters between solid sediment and solution were also fitted using the DIFS (DGT-induced fluxes in sediments) model. The results suggested that Fe-bound P (Fe-P) was the dominant pool which contributed to the resupply potential of P in the water-sediment continuum. Significant upward decreases of labile PDGT, Fe2+DGT, and S2-DGT fluxes were detected in pristine and incubated microcosms. This dominance indicated the more obvious immobilization of labile P via oxidation of both Fe2+ and S2- in oxidic conditions. Additionally, these labile analytes in the microcosms obviously decreased after a 30-day incubation period, indicating that water-level fluctuations can significantly regulate adsorption-desorption processes of the P bound to Fe-containing minerals within a short time. Higher concentrations of labile PDGT, Fe2+DGT, and S2-DGT were measured at the shallow lake region where more drastic water-level variation occurred. This demonstrates that frequent adsorption-desorption of phosphate from the sediment particles to the aqueous solution can result in looser binding on the solid sediment surface and easier desorption in aerobic conditions via the regulation of water levels. Higher R values fitted with DIFS model suggested that more significant desorption and replenishment effect of labile P to the aqueous solution would occur in lake regions with more dramatic water-level variations. Finally, a significant positive correlation between S2-DGT and Fe2+DGT in the sediment indicated that the S2- oxidization under the conditions of low water-level can trigger the reduction of Fe(III) and subsequent release of active P. In general, speaking, frequent water-level fluctuations in the lake over time facilitated the formation and retention of the Fe(II) phase in the sediment, and desorption of Fe coupled P into the aqueous solution when the water level was high.

Characterization and source identification of organic phosphorus in sediments of a hypereutrophic lake.

High phosphorus (P) load and consequent algal bloom are critical issues because of their harmful effects to aquatic ecosystems. The organic phosphorus (Po) cycling and hydrolyzation pathway in the sediments of a hypereutrophic lake area with high algae biomass were investigated using stable isotopes (δ13C and δ15N) along with C/N ratios, a sequential extraction procedure, 31P NMR spectrum, and alkaline phosphatase activity (APA) was measured simultaneously. C/N ratios lower than 10 combined with lighter δ13C (-23.5 to -25.2‰) and δ15N values (3.7-9.5‰) indicated that endogenous algal debris contributed to the predominant proportions of P-containing organic matter in the sediments. Sequential extraction results showed that Po fractions decreased as nonlabile Po > moderately labile Po > biomass-Po. Decreasing humic-associated Po (HA-Po) in sediments downward suggested the degradation of high-molecular-weight Po compounds on the geological time scale to low-molecular-weight Po including fulvic-associated Po (FA-Po), which is an important source of labile Po in the sediment. An analysis of the solution 31P NMR spectrum analysis showed that important Po compound groups decreased in the order of orthophosphate monoesters > DNA-Po > phospholipids. The significant correlation indicated that orthophosphate monoesters were the predominant components of HA-Po. Rapid hydrolysis of labile orthophosphate diesters further facilitated the accumulation of orthophosphate monoesters in the sediments. Additionally, the simultaneously upward increasing trend demonstrated that APA accelerated the mineralization of Po into dissolved reactive phosphorus (DRP), which might feed back to eutrophication in algae-dominant lakes. The significantly low half-life time (T1/2) for important Po compound groups indicated faster metabolism processes, including hydrolysis and mineralization, in hypereutrophic lakes with high algae biomass. These findings provided improved insights for better understanding of the origin and cycling processes as well as management of Po in hypereutrophic lakes.

Assessment of nutrients and heavy metals enrichment in surface sediments from Taihu Lake, a eutrophic shallow lake in China.

Concentrations of the nutrients (TN and TP), phosphorus fractions and heavy metals (Co, Cr, Cu, Mn, Ni, Pb, Sr, Ti, V, Zn and Hg) in 40 surface sediment samples collected from Taihu Lake, a eutrophic shallow lake in China, were determined. The results showed that the northwest region of the lake possessed higher concentrations of TN and TP, as well as the similar spatial distribution trend in the water column. This should be related to excessive anthropogenic input from industrial effluents and domestic sewage in surrounding areas. Similarly, the concentrations of P fractions exhibited significant regularity. In addition, except for Sr showing low concentration, the rest of the heavy metals in the surface sediments had two- to four-folds of magnitude of the concentrations compared with the reference values in earth's crust. In the past decade, concentrations of heavy metals had undergone different levels of variations. Principal component analysis (PCA) and enrichment factors (EFs) of the compositional data aiming at heavy metals showed that Taihu Lake was slightly exposing to heavy metal contamination except Sr. High concentrations of heavy metals were ascribed to the discharge of untreated and partially treated industrial waste water via rivers. Co, Cr, Cu, Mn, Ni, Pb, V and Zn positively correlated with each other (R = 0.78-0.92), that indicated they had analogous sources and/or kindred geochemistry characteristics. Differing from nutrients, randomness in the space indicated that heavy metals had a complex distribution.

[Space distribution characteristics and diversity analysis of phosphorus from overlying water and surface sediments in Taihu Lake].

The physi-chemical indexes in the overlying water and surface sediments of Taihu Lake, an eutrophic shallow lake, were determined. Then, the isopleth maps of spatial distribution of each parameter were illustrated. The results show that the concentrations of SRP, TP and TN in the overlying water and TOC, TN and TP as well as phosphorus fractions in surface sediments exhibit distinct diversity in spatially. The lowest values of TP and TN were 0.05, 0.88 mg x L(-1), respectively. The concentrations of Fe-P ranged from 29.13 to 258.31 mg x kg(-1). Besides, the northwest lake regions, high-load Ca-P was surveyed in the South Taihu Lake and East Taihu Lake with the highest value of 357.68 mg x kg(-1). The highest concentration of OP, 371.91 mg x kg(-1) was detected in the northwest region of the lake. IP takes up a greater proportion of TP than OP, and the highest value is approximately 50% higher than the lowest value. Fe-P has higher percentage in IP compared with Ca-P. Significant correlation between Fe-P, SRP and TP showed that Fe-P was the important phosphorus source of the overlying water (R: 0.49, 0.64). Furthermore, high correlation coefficients between TOC, TOC, C/N, TN, TP and phosphorus fractions suggest that higher concentration of organics was favor to the accumulation and burial of nutrients. The high-load contaminants exist principally in the Zhushan Bay, Wulihu Lake, Meiliang Bay and the northwest region of Taihu Lake. Significant heterogeneity of nutrients distribution in space of Taihu Lake connects with direct action of emission load of sewage. Simultaneously, different biogeochemical behaviors of each parameter play an important role.

Characteristics of phosphorus fractionated from the sediment resuspension in abrupt expansion flow experiments.

Phosphorous (P) fraction characteristics in sediment resuspension were investigated under adequately hydrodynamic conditions. Four forms of P in overlying water, including dissolved inorganic P, dissolved total P, total P, and particulate P, and six fractions of P in suspended particulate matter (SPM), including loosely sorbed P (NH4Cl-P), redox-sensitive P (BD-P), aluminum-bound P (Al-P), organic P (NaOH-nrP), calcium-bound P (Ca-P) and residual P (Res-P), were quantified, respectively. Different hydrodynamic conditions resulted in different P form changes. Four states could be ascribed: (1) P desorption by sediment and SPM, and P adsorption by overlying water; (2) P desorption by SPM, and P adsorption by overlying water; (3) P adsorption by SPM, and P desorption by overlying water; and (4) P equilibrium between SPM and overlying water. The contents of P in overlying water acquired peak values in the middle position of the vertical P distribution due to the combined actions of SPM and sediment. P fractions in SPM were in the following order: BD-P > NaOH-nrp > Ca-P > Al-P > Res-P > NH4Cl-P. BD-P in SPM frequently exchanged with P forms in overlying water. Resuspension was favorable to forming Ca-P in SPM.