Mercury distribution in Douro estuary (Portugal)

Determinations of dissolved reactive and total dissolved mercury, particulate and sedimentary mercury, dissolved organic carbon (DOC), particulate organic carbon (POC) and suspended particulate matter (SPM) have been made in the estuary of river Douro, in northern Portugal. The estuary was stratified by salinity along most of its length, it had low concentrations of SPM, typically <20 mg dm(-3), and concentrations of DOC in the range <1.0-1.8 mg dm(-3). The surface waters had a maximum dissolved concentration of reactive mercury of about 10 ng dm(-3), whereas for the more saline bottom waters it was about 65 ng dm(-3). The surface waters had maximum concentrations of total suspended particulate mercury of approximately 7 microg g(-1) and the bottom waters were always <1 microg g(-1). Concentrations of mercury in sediments was low and in the range from 0.06 to 0.18 microg g(-1). The transport of mercury in surface waters was mainly associated with organic-rich particulate matter, while in bottom waters the dissolved phase transport of mercury is more important. Lower particulate organic matter, formation of chlorocomplexes in more saline waters and eventually the presence of colloids appear to explain the difference of mercury partitioning in Douro estuarine waters.     

Sources of particulate and dissolved organic carbon in the St Lawrence River: isotopic approach

We investigate sources of both dissolved and particulate organic carbon in the St Lawrence River from its source (the Great Lakes outlet) to its estuary, as well as in two of its tributaries. Special attention is given to seasonal interannual patterns by using data collected on a bi‐monthly basis from mid‐1998 to mid‐2003. δ¹³C measurements in dissolved inorganic carbon, dissolved organic carbon (DOC) and particulate organic carbon (POC), as well as molar C : N in particulate organic matter (POM), are used to bring insight into the dynamic between aquatic versus terrigenous sources. In addition, ¹⁴C activities of DOC were measured at the outlet of the St Lawrence River to its estuary to assess a mean age of the DOC exported to the estuary. In the St Lawrence River itself, aquatically produced POC dominates terrestrially derived POC and is depleted in ¹³C by approximately 12‰ versus dissolved CO₂. In the Ottawa River, the St Lawrence River's most important tributary, the present dataset did not allow for convincing deciphering of POC sources. In a small tributary of the St Lawrence River, aquatically produced POC dominates in summer and terrestrially derived POC dominates in winter. DOC seems to be dominated by terrestrially derived organic matter at all sampling sites, with some influence of DOC derived from aquatically produced POC in summer in the St Lawrence River at the outlet of the Great Lakes and in one of its small tributaries. The overall bulk DOC is relatively recent (¹⁴C generally exceeding 100% modern carbon) in the St Lawrence River at its outlet to the estuary, suggesting that it derives mainly from recent organic matter from topsoils in the watershed. Copyright © 2005 John Wiley & Sons, Ltd.     

Riverine inputs of total organic carbon and suspended particulate matter from the Pearl River Delta to the coastal ocean off South China

A total of 1008 samples were collected from the eight major riverine runoff outlets in the Pearl River Delta (PRD) during 2005-2006 to estimate the fluxes of total organic carbon (TOC) to the coastal ocean off South China. The average dissolved organic carbon (DOC) concentration was 1.67 mg/L with a range of 1.38-2.13 mg/L. Concentrations of particulate organic carbon (POC) ranged from 2.66-4.12% of total suspended particulate matter (SPM). The fluxes of TOC and SPM from the PRD via the eight outlets were 9.2 x 10(5) and 2.5 x 10(7)tons/yr, respectively. Temporal variations in POC and DOC were observed at all outlets due to the large variability in runoff levels because of the seasonality of rainfall, and the riverine discharge amount was an important factor controlling TOC flux. The net contribution of organic carbon from the PRD to the coastal ocean represented approximately 0.1-0.2% of total organic carbon transported by rivers worldwide.     

Estimation of particulate organic carbon flux in relation to photosynthetic production in a shallow coastal area in the Seto Inland Sea

Sediment trap experiments were carried out three times from 1999 to 2000, in the western part of the Seto Inland Sea (Suo-Sound), Japan. We investigated both the particulate flux and the composition of chemical substances in the sediment trap samples. Based on the results, we discuss the origin of particulate organic carbon (POC) collected by the sediment traps in a coastal area. Moreover, we purposed to estimate the flux of the portion of the POC that is derived from phytoplankton photosynthesis. The fluxes of POC varied between 677 and 3424 mgC m(-2) d(-1). Significant positive correlations between POC and aluminum (Al) fluxes suggested that these components show almost the same behaviour. The mean value of the Al flux was about eight times higher than that of Al burial rates on the sediment surface. Therefore, it seems that the POC flux observed with the sediment traps was considerably overestimated. Moreover, judging from the fact that Al is a typical terriginous element, it seems that most of the POC collected in the sediment traps derived from the re-suspended surface sediment or sediment transported laterally from shallow flanks such as intertidal mudflats. The fluxes of chlorophyll a (Chl a) were independent of the POC fluxes, and a relatively consistent correlation was found between Chl a abundance in the water column and the Chl a flux. Moreover, surface sediment Chl a content was approximately 100 times lower than that of suspended matter. Therefore, resuspension and terriginous contributions to Chl a collected in sediment traps are likely to be negligible. The POC content in the trap samples varied between 22.4 and 70.7 mg g(-1) dry weight. The variations of POC contents were positively correlated with the Chl a contents: POC(mg g(-1))=76.5 x Chl a(mg g(-1)) + 26.0 (r=0.95, p<0.01, n=9). This result shows that POC contents strongly corresponded with phytoplankton and their debris. It was also considered that the fraction of POC derived from phytoplankton primary production could be estimated as Chl a content times a certain factor. In this study, we estimated the flux of the portion of the POC originating from phytoplankton production by multiplying the Chl a fluxes by 76.5 (the mean POC:Chl a ratio in the trap samples). These values varied between 308 and 758 mgC m(-2) d(-1), and accounted for 35.1+/-21.2% of total POC flux. Although the amount of POC that originates from phytoplankton photosynthesis was a small portion of total POC flux, it seems to be a large portion of potential primary production in the water column.     

Dynamics and fluxes of organic carbon and nitrogen in two Guiana Shield river basins impacted by deforestation and mining activities

Deforestation and mining activities have proven to be very damaging to rivers because these activities disturb the environmental characteristics of rivers. Thus, the concentrations of dissolved organic carbon (DOC), particulate organic carbon (POC), particulate nitrogen (PN), and Chlorophyll‐a (Chl‐a) were measured monthly during 2 hydrological years in the Maroni and Oyapock Rivers to assess the dynamics and fluxes of organic carbon and nitrogen in these 2 Guiana Shield basins, which have been strongly (Maroni) and weakly (Oyapock) impacted by deforestation and mining activities. The 2‐year time series show that DOC, POC, PN, and Chl‐a concentrations vary seasonally with discharge in both rivers, indicating a hydrologically dominated control. Temporal patterns of DOC, POC, and PN indicate that these variables show maximum concentrations in rising waters due to the yield of organic matter and nitrogen accumulated in soils, which are incorporated into the rivers during rainfall. However, the Chl‐a concentrations were at a maximum during low‐water stages. The C/N and C/Chl‐a ratios also showed a seasonal trend, with lower values during the low water periods due to an increase in algal biomass. During high water, the POC in both rivers is the result of terrestrial organic matter, whereas during low‐water autochthonous organic matter can reach up to 34% of the POC. The mean annual fluxes of TOC and PN were higher (4.56 × 10⁵ tonC year^?1 and 1.77 × 10⁴ tonN year^?1, respectively) in the Maroni River than those (1.84 × 10⁵ tonC year^?1 and 0.54 × 10⁴ tonN year^?1, respectively) in the Oyapock River. However, the specific fluxes of DOC, POC, and PN from both basins were nearly the same. Although gold mining activities are performed in both basins, there is no conclusive evidence regarding the impact of these activities on the dynamics of organic matter and particulate nitrogen in the Maroni and Oyapock Rivers.     

Total organic carbon fluxes of the Red River system (Vietnam)

Riverine transport of organic carbon from terrestrial ecosystems to the oceans plays an important role in the global carbon cycle. The Red River is located in Southeast Asia where river discharge, sediment loads and fluxes of elements (carbon, nitrogen and phosphorus) associated with suspended solids have been dramatically altered over past decades as a result of reservoir impoundment and land use, population, and climate change. Dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations were measured monthly at four stations of the Red River system from January 2008 to December 2010. The results reveal that POC changed synchronically with total suspended solids (TSS) concentration and with the river discharge, whereas no clear trend was observed for DOC concentration. The mean value of total organic carbon (TOC = DOC + POC) flux in the delta of the Red River was 31.5 × 10¹³ ± 4.0 × 10¹³ MgC.yr^?1 (range 27.9–35.8 × 10¹³ MgC.yr^?1 which leads to a specific TOC flux of 2012 ± 255 kgC.km^?2.yr^?1 during this 2008–2010 period. About 80% of the TOC flux was transferred to the estuary during the rainy season as a consequence of the higher river water discharge. The high mean value of the POC:Chl‐a ratio (1585 ± 870 mgC.mgChl‐a^?1) and the moderate C:N ratio (7.3 ± 0.1) in the water column system suggest that organic carbon in the Red River system is mainly derived from erosion and soil leaching in the basin. The effect of two new dam impoundments in the Red River was also observable with lower TOC fluxes in 2010 compared with 2008. Copyright © 2017 John Wiley & Sons, Ltd.     

Composition and flux of suspended organic matter in the middle and lower reaches of the Changjiang (Yangtze River) — impact of the Three Gorges Dam and the role of tributaries and channel erosion

To investigate the sources of particulate organic matter (POM) and the impact of Three Gorges Dam (TGD), two large lakes and erosion processes on determining the composition and flux of POM in low water discharge periods along the middle and lower Changjiang, suspended particulate samples were collected along the middle and lower reaches of the Changjiang (Yangtze River) in January 2008. Organic geochemistry of bulk sediment (particulate organic carbon, organic carbon to nitrogen molar ratio (C/N), stable carbon isotope (δ¹³C) and grain size) and biomarker of bulk sediment (lignin phenols) were measured to trace the sources of POM. The range of C/N ratios (6.4–8.9), δ¹³C (?24.3‰ – ?26.2‰) and lignin phenols concentration Λ8 (0.45 mg/100 mg OC‐2.00 mg/100 mg OC) of POM suggested that POM originated from the mixture of soil, plant tissue and autochthonous organic matter (OM) during the dry season. POM from lakes contained a higher portion of terrestrial OM than the mainstream, which was related to sand mining and hydropower erosion processes. A three end‐member model based on δ¹³C and Λ8 was performed. The results indicated that soil contributed approximately 50% of OM to the POM, which is the dominant OM source in most stations. POM composition was affected by total suspended matter (TSM) and grain size composition, and the direct OM input from two lakes and channel erosion induced OM. The lower TSM concentration in January 2008 was mainly caused by seasonal variations; the impact from the TGD in the dry season was relatively small. A box model indicated that more than 90% of the terrestrial OM transported by the Changjiang in January 2008 was from the middle and lower drainage basins. Channel erosion induced OM, and contributions from Poyang Lake were the major terrestrial OM sources in the dry season. Copyright © 2012 John Wiley & Sons, Ltd.     

UV spectrometry for measuring particulate organic matter in natural water

Ultraviolet (UV) spectra were measured to characterize the dissolved and particulate organic matter in a bog and to investigate the seasonal fluctuation of this organic matter. The optical density spectra in the UV region of dissolved organic matter (DOM) were proportional to ^–4, where is the wavelength of incident light. There was also small absorption on the ^–4 spectra. The optical density at a wavelength of 280 nm was proportional to the concentration of dissolved organic carbon (DOC). The spectra and the dependency of optical density on DOC did not vary throughout the investigation period. The UV spectra of acid extractions of particulate organic matter (POM) showed two absorption peaks at the wavelengths of 220 nm and 335 nm. These peaks are well represented by the sum of two Lorentz functions. The ratio of the absorbances,A ₂₈₀/A ₃₃₅, was dependent on the nitrogen/carbon ratio of POM and the chlorophyll fraction in particulate organic carbon (POC), and not dependent on POC itself. The dependency of POC absorption at 280 nm varied with this ratio which fluctuated seasonally.     

Towards understanding organic matter fluxes and reactivity in surface waters: Filtering impact on DOC and POC degradation

Peatlands cover a very small area of the Earth, but store globally significant quantities of carbon and export disproportionate quantities of fluvial organic carbon, especially when the peatlands are degraded or disturbed. Peatland headwater catchments with high concentrations of dissolved and particulate organic carbon (DOC and POC) provide an opportunity to investigate the possibility of competing effects that could lead to enhanced or diminished turnover of DOC in the presence of POC. Both POC and DOC can be degraded by light and microbes, producing smaller molecules and releasing CO₂ and CH₄ to the atmosphere, and POC can inhibit light penetration, stabilize DOC by providing adsorption sites and providing surfaces for microbes to interact with DOC. However, the majority of peatland fluvial carbon studies are conducted using filtered water samples, and measure only the DOC concentration, so the impact of the particulate organic matter (POM) on in-stream processing of organic carbon is relatively unknown. It is therefore possible that studies have underestimated carbon transformations in rivers as they have not considered the interaction of the particulate material on the dissolved concentrations; there could be higher losses than previously estimated, increasing the contribution of peatland headwaters to GHG emissions. In this study, we assessed if the current approach of DOC degradation studies accurately represent the impact of POM on DOC degradation, by quantifying DOC production from POM, and therefore POC, over time in water with manipulated POM concentrations. Both filtered and unfiltered water lost 60% of the DOC over 70 hours, whereas the treatment with additional POM lost only 35%. The results showed that filtering does not significantly impact the DOC degradation rates; however, when the POC concentration was doubled, there was a significant reduction in DOC degradation, suggesting that filtering would still be necessary to get accurate rates of DOC transformations in waters with high POC concentrations.     

Sediments, nutrients and pesticide residues in event flow conditions in streams of the Mackay Whitsunday Region, Australia

The Mackay Whitsunday region covers 9000 km(2) in northeastern Australia. A study of diffuse pollutants during high flow events was conducted in coastal streams in this region. Sampling was conducted in the Pioneer River catchment during a high flow event in February 2002 and in Gooseponds Creek, Sandy Creek and Carmila Creek in March 2003. Concentrations of five herbicides; atrazine (1.3 microg l(-1)), diuron (8.5 microg l(-1)), 2,4-D (0.4 microg l(-1)), hexazinone (0.3 microg l(-1)) and ametryn (0.3 microg l(-1)) and high concentrations of nutrients (total nitrogen 1.14 mg l(-1), total phosphorus 0.20 mg l(-1)) and suspended sediments (620 mg l(-1)) were measured at Dumbleton Weir on the lower reaches of the Pioneer River. Drinking water guidelines for atrazine and 2,4-D were exceeded at Dumbleton Weir, low reliability trigger values for ecosystem protection for diuron were exceeded at three sites and primary industry guidelines for irrigation levels of diuron were also exceeded at Dumbleton Weir. Similar concentrations were found in the three smaller streams measured in 2003. Herbicides and fertilisers used in sugarcane cultivation were identified as the most likely major source of the herbicide residues and nutrients found.     

Organic carbon deliveries and their flow related dynamics in the Fitzroy estuary

The Fitzroy estuary (Queensland, Australia) receives large, but highly episodic, river flows from a catchment (144,000 km(2)) which has undergone major land clearing. Large quantities of suspended sediments, and particulate and dissolved organic carbon are delivered. At peak flows, delta(13)C (-21.7+/-0.8 per thousand) and C/N (14.8+/-1.3) of the suspended solids indicate that the particulate organic material entering the estuary is principally soil organic carbon. At the lower beginning flows the particulate organic matter comes from in-stream producers (delta(13)C=-26 per thousand). The DOC load is about 10 times the POC load. Using the inverse method, budgets for POC and DOC were constructed for high and low flows. Under high flows, only a small portion of the POC and DOC load is lost in the estuary. Under dry season (low flow) conditions the estuary is a sink for DOC, but remains a source of POC to the coastal waters.     

Comparison of C and N stable isotope ratios between surface particulate organic matter and microphytoplankton in the Gulf of Lions (NW Mediterranean)

Carbon and nitrogen stable isotope ratios of particulate organic matter (POM) in surface water and 63–200 μm-sized microphytoplankton collected at the fluorescence maximum were studied in four sites in the Gulf of Lions (NW Mediterranean), a marine area influenced by the Rhone River inputs, in May and November 2004. Some environmental (temperature, salinity) and biological (POM, Chlorophyll a and phaeopigments contents, phytoplankton biomass and composition) parameters were also analysed. Significantly different C and N isotopic signatures between surface water POM and microphytoplankton were recorded in all sites and seasons. Surface water POM presented systematically lower δ¹³C (∼4.2‰) and higher δ¹⁵N (∼2.8‰) values than those of microphytoplankton, due to a higher content of continental and detrital material. Seasonal variations were observed for all environmental and biological parameters, except salinity. Water temperature was lower in May than in November, the fluorescence maximum was located deeper and the Chlorophyll a content and the phytoplankton biomass were higher, along with low PON/Chl a ratio, corresponding to spring bloom conditions. At all sites and seasons, diatoms dominated the phytoplankton community in abundance, whereas dinoflagellate importance increased in autumn particularly in coastal sites. C and N isotopic signatures of phytoplankton did not vary with season. However, the δ¹⁵N of surface water POM was significantly higher in November than in May in all sites likely in relation to an increase in ¹⁵N/¹⁴N ratio of the Rhone River POM which influenced surface water in the Gulf of Lions. As it is important to determine true baseline values of primary producers for analysing marine food webs, this study demonstrated that C and N isotopic values of surface water POM cannot be used as phytoplankton proxy in coastal areas submitted to high river inputs.     

Copper speciation survey from UK marinas, harbours and estuaries

The use of copper in antifouling paints has increased in the UK in the last 20 years as TBT and several other organic biocides have been phased out. To assess the probable impact of copper on estuarine systems a survey was undertaken to measure the different fractions of copper present in the water column at current usage. The different fractions measured were; labile copper, (LCu) considered as both the free copper ions and inorganically bound copper, the total dissolved copper (TDCu) present, and the difference between them taken as the organically bound likely non-toxic copper fraction. The survey considered sites with different levels of boat use, namely marinas, harbours and estuaries, differing physical parameters of suspended and dissolved organic matter, different seasons of the year and different depths in the water column all of which control speciation behaviour. Suspended particulate matter (SPM) values were measured at all sites and increased from West to East coast locations (5.7-34.4 mg/l). Dissolved organic matter (DOM) values ranged from 0.58 to 2.2mg/l C. The total dissolved copper concentrations ranged from 0.30 to 6.68 microg/l, with labile fraction ranging from 0.02 to 2.69 microg/l, and most labile copper concentrations below 1 microg/l. None of the yearly mean copper measurements exceeded the 76/464/EEC EQS of 5 microg/l. Of the 306 measurements, only one dissolved copper value in one season was above 5 microg/l. This ratio of labile to total copper was between 10 and 30%. The results from this survey suggest that if toxicity of copper is due to the labile fraction then using the total dissolved copper concentrations as an indicator of impact overestimate the risk by a factor of four times.     

Particulate carbon and nitrogen dynamics in a headwater catchment in Northern Thailand: hysteresis,high yields,and hot spots

Rivers of South and Southeast Asia disgorge large suspended sediment loads, reflecting exceptionally high rates of erosion promoted by natural processes (tectonic and climatic) and anthropogenic (land‐use change) activities that are characteristic of the region. While particulate carbon and nitrogen fluxes have been characterized in some large Asian rivers, less is known about the headwater systems where much sediment and organic material are initially mobilized. This study, conducted in the 74‐km² Mae Sa Experimental Catchment in northern Thailand, shows that the Sa River is an important source for particulate organic carbon (POC) and particulate organic nitrogen (PON) transported to larger river systems and downstream reservoirs. However, the yields during three years of investigation varied greatly: 5.0–22.3 Mg POC km^?2 y^?1 and 0.48–2.02 Mg PON km^?2 y^?1. The 22.3 Mg POC km^?2 y^?1 yield is the highest reported for any river on the Asian continent. Stream samples collected during 12 storms showed that almost 3% of the total suspended solid load is POC 0.7 µm to 2.0 mm in size. This percentage is higher than other values for most large rivers on the continent. Further, we documented a strong pulse hysteretic behaviour in the stream, whereby peak fluxes of POC and PON are often delayed (anticlockwise hysteresis) or accelerated (clockwise hysteresis) relative to stream flow peaks (or are complex), complicating the prediction of storm‐based or annual particulate carbon and nitrogen fluxes. Stream turbidity and total suspended sediment are reasonable proxies for POC and PON concentrations, while stream discharge is not a good predictor variable. Observed C:N ratios for measured particulate samples range from 3 to 83, with the high‐end values likely associated with fresh (non‐decomposed) vegetative material greater than 2 mm in diameter. The C:N ratio (weighted based on three sediment sizes) for 12 events ranges from 7.5 to 15.3. These modest values reflect the relatively low C:N ratios for small size fractions (0.7–0.63 µm) that comprise 50–90% of the TSS load in the events. Overall, organic material <0.63 µm contribute about 75% of the total POC load and 80% of the PON load. The annual C:N ratio for the river is approximately 10–11. Collectively, our findings indicate the occasionally high yields make the Sa River—and potentially other similar headwater rivers—a hot spot for POC and PON transported to downstream water bodies. Complex hysteresis patterns and high year‐to‐year variability hinders our ability to calculate and predict these yields without continuous, automated monitoring of discharge and turbidity. Copyright © 2016 John Wiley & Sons, Ltd.     

The effect of Hurricane Lili on the distribution of organic matter along the inner Louisiana shelf (Gulf of Mexico,USA)

On October 3, 2002 Hurricane Lili made landfall on a previously studied region of the inner Louisiana shelf as a Category 2 storm with winds over 160 km/h. A week after the hurricane, major impacts of the storm were not evident in the water column except for the lower than expected inshore salinities (∼12 psu) for this time of year, which was characterized by low river discharge. Turbidity profiles were typical of those measured during previous investigations with suspended sediment concentrations >75 mg/L at inshore stations and <50 mg/L in surface waters and offshore. The implication is that the sediments resuspended during the hurricane settled soon after the storm passage. Water column particulate organic carbon (POC) concentrations ranged from 0.1 to over 2.0 mg/L, with the highest concentrations measured near the seabed and in the inshore portions of the study area. Suspended particles were characterized by low organic matter content (%POC of 0.5–2 wt%), low chlorophyll:POC ratios (Chl:POC<4 mg/g) and moderately elevated POC:particulate nitrogen ratios (POC:PN of 10–14 mol/mol), all suggesting their source was locally resuspended seabed sediment rather than from algal biomass or land-derived vascular plant detritus.Post hurricane sediment deposition throughout the study area resulted in a storm layer that ranged from <0.5 to 20 cm in thickness. In most locations sediment accumulation ranged from 3 to 10 cm. The storm deposits were generally composed of silty clays with a coarser, somewhat sandy 1–2 cm basal layer. Surface sediments from the storm layer were characterized by relatively high mineral surface areas (SA of 30–50 m²/g) and elevated OC contents (%OC of 1.0–2.0%). The dispersal of fine sediments following the hurricane resulted in marked changes in the SA and %OC values of surface sediments from offshore locations, which prior to the storm contained coarser, organic-poor particles (SA of 5–15 m²/g and %OC of 0.2–0.6%). The OC:SA and OC:N ratios of storm layer sediments ranged from 0.4 to 0.6 mg OC/m² and from 10 to 12 mol/mol, respectively, and were comparable to those measured in surface sediments prior to the hurricane. Such similarities in the composition of the organic matter reinforce the idea that the source of the storm deposits was the finer fraction of resuspended seabed sediments, with little evidence for inputs from local land-derived sources or autochthonous algal production. Overall, the magnitude of sediment and organic matter deposition on the seabed after the storm greatly exceeded the annual inputs from the Atchafalaya River and coastal primary production. The combined effects of hurricane-driven erosion and post-storm deposition represent a major perturbation to the benthic community of the region, which is already subject to these types of disturbances due to the combined effects of peaks in river discharge and the passage of storm fronts.     

Total Organic Carbon (TOC) as a Sum Parameter of Water Pollution in Selected Polish Rivers (Vistula,Odra, and Warta)

This paper reports on total organic carbon (TOC) and its fractions dissolved organic carbon (DOC) and particulate organic carbon (POC) studied in different Polish rivers. The samples investigated came from the Vistula, Odra, and Warta rivers, and were compared with similar data on river waters available in the literature. The DOC concentrations ranged from 10.0 to 14.2 mg/L and did not vary during the vegetative season. The POC values considerably increased from May through September and reached a maximum in summer. Results for the years 1991τ1996 evidenced a significant increase in the POC value for the Polish rivers from 10.8 to 24.5 mg/L, in comparison with analogous values for West European rivers and North American ones. The enhanced values of TOC and POC were interpreted as being due to anthropogenic pollution.     

Phosphorus Forms and Their Changes in Water of Three Subalpine Lakes in Italy

Total phosphorus and its main forms: dissolved mineral, dissolved organic, particulate organic and particulate mineral in the vertical water column of three subalpine lakes of various types in Italy, has been estimated during the winter-vernal season. The range of variation in the phosphorus content in these waters was as follows: total phosphorus 16 ± 2860 μg/1 PO₄, dissolved mineral phosphorus 4 ± 1040 μg/l PO₄, dissolved organic phosphorus 1 ± 160μg/l PO₄, particulate organic phosphorus 0 ± 290 μg/l PO₄ and particulate mineral phosphorus 1 ± 100 μg/l PO₄, Generally the content of total phosphorus and dissolved mineral phosphorus (phosphates) increased with the degree of eutrophy with the depth and with the progress of the vernal season towards the summer stagnation time. The amount of phosphates increased in water with the depletion of oxygen, both in the verical water column and with the progress of stagnation time. The amounts of dissolved organic phosphorus decressed with the depth of the vertical water column whereas the dissolved mineral phosphorus increased. The development of the particulate organic phosphorus stratification in the vertical water column was clearly visible in the eutrophic lake. The quantities of total phosphorus and its main component, dissolved mineral phosphorus, decreased evidently from January to May in all three lakes, mostly in the eutrophic lake. The reason of this decrease is sorption by lake sediments and to a certain degree sedimentation of phosphorus sorbed by ferric hydroxide. The increase of dissolved mineral phosphorus and that of total phosphorus in the vertical water column and with the progress of summer stagnation had as a reason the liberation of phosphorus from sediments, and not so much decomposition of sedimentating plankton or dissolved organic phosphorus. The share of single (mean) values of phosphorus forms in the total phosphorus was as follows: In the oligotrophic lake the share of particulate mineral phosphorus was extremely high in March (21% of the total), probably because of the inflow of the melting waters from the drainage area. The development of vertical stratification in waters of three subalpine Italian lakes at the end of the vernal season (May) indicates the quantitative prevailing of dissolved mineral phosphorus with its increase with the depth and domination of dissolved organic phosphorus in the trophogenic zone.     

Seasonal and spatial variation in suspended matter,organic carbon,nitrogen, and nutrient concentrations of the Senegal River in West Africa

The Senegal River is of intermediate size accommodating at present about 3.5 million inhabitants in its catchment. Its upstream tributaries flow through different climatic zones from the wet tropics in the source area in Guinea to the dry Sahel region at the border between Senegal and Mauritania. Total suspended matter, particulate and dissolved organic carbon and nitrogen as well as nutrient concentrations were determined during the dry and wet seasons at 19 locations from the up- to downstream river basin. The aims of the study were to evaluate the degree of human interference, to determine the dissolved and particulate river discharges into the coastal sea and to supply data to validate model results. Statistical analyses showed that samples from the wet and dry season are significantly different in composition and that the upstream tributaries differ mainly in their silicate and suspended matter contents. Nutrient concentrations are relatively low in the river basin, indicating low human impact. Increasing nitrate concentrations, however, show the growing agriculture in the irrigated downstream areas. Particulate organic matter is dominated by C4 plants during the wet season and by aquatic plankton during the dry season. The total suspended matter (TSM) discharge at the main gauging station Bakel was about 1.93 Tg yr⁻¹ which is in the range of the only available literature data from the 1980s. The calculated annual discharges of particulate organic carbon (POC), dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) are 55.8 Gg yr⁻¹, 54.1 Gg yr⁻¹, and 5.3 Gg yr⁻¹, respectively. These first estimates from the Senegal River need to be verified by further studies.     

2005-2017年北部太湖水体叶绿素a和营养盐变化及影响因素

利用国家生态观测网络太湖湖泊生态系统研究站对北部太湖14个监测点2005-2017年的营养盐和叶绿素a浓度逐月监测数据,分析了北部太湖2005年以来水体营养盐和叶绿素a变化特征,探讨了叶绿素变化的影响因素.结果表明,2015年以来,北部太湖水体叶绿素a浓度呈现显著增高特征,特别是5-7月的蓝藻水华灾害关键期,水体叶绿素a浓度增幅更加明显;营养盐方面,氮、磷对治理的响应完全不同：水体总氮、溶解性总氮、氨氮的降幅很明显,甚至在春末夏初的蓝藻生长旺盛期出现了供给不足的征兆;但水体总磷降幅却不明显,加之蓝藻水华的磷"泵吸作用",近3 a来水体总磷浓度反而有升高趋势,溶解性总磷浓度也无明显下降趋势.不同湖区的营养盐变化也不相同：西北湖区溶解性总氮、溶解性总磷浓度显著高于梅梁湾、贡湖湾和湖心区,而且后3个湖区的水质呈现均一化趋势.统计分析表明,北部太湖水体叶绿素a浓度与颗粒氮、颗粒磷、总磷、高锰酸盐指数均呈显著正相关,与溶解态氮呈负相关;5-7月水华关键期北部太湖水体叶绿素a浓度与上半年（1-6月）逐日水温积温、总降雨量、年平均水位均呈显著正相关关系.从研究结果可以看出,近年来北部太湖水体叶绿素a浓度的波动很大程度上受水文气象因子的影响;2007年以来太湖流域一系列生态修复工程的实施,虽然明显降低了湖泊氮浓度,但由于流域和湖体的氮磷本底较高,磷的缓冲能力大,致使水体营养盐水平仍未降到能显著抑制蓝藻生长的水平,年际之间的水文气象条件差异成为蓝藻水华暴发强度差异的主控因素.为此,仍需加大对太湖流域氮、磷负荷的削减,使湖体氮、磷浓度降低到能显著影响蓝藻生长的水平,才能摆脱水文气象条件对蓝藻水华情势的决定作用.     

The sources and seasonal fluxes of particulate organic carbon in the Yellow River

The Yellow River transports a large amount of sediment and particulate organic carbon (POC), which is thought to mainly derive from erosion of the Chinese Loess Plateau (CLP). However, the compositions, sources and erosional fluxes of POC in the Yellow River remain poorly constrained. Here we combined measurements of mineralogy, total organic carbon content (OC_total), stable organic carbon isotopes (δ¹³C_org), radiocarbon (¹⁴C) activity of organic matter in bulk suspended sediments collected seasonally from the upper and middle Yellow River, to quantify the compositions and fluxes of the POC and to assess its sources (biospheric and petrogenic POC, i.e. POC_bio and POC_petro, respectively). The results showed that the POC loading of sediments was controlled by mineralogy, grain size and specific surface area of loess particles. The F_mod of POC (0.71 to 0.31) can be explained by mixing of POC_petro with modern and aged POC_bio. A binary mixing model based on the hyperbolic relationship of the F_mod and OC_total revealed a wide range of ages of POC_bio from 1300 to 11100 ¹⁴C years. Relative to the upstream station, the annual POC_bio and POC_petro fluxes in the Yellow River are more than doubled after it flows crossing the CLP within 35% drainage area gain, resulting in POC_bio and POC_petro yields of the CLP at 3.50 ± 0.59 and 0.48 ± 0.49 tC/km²/yr, respectively. POC flux seasonal variation revealed that monsoon rainfall exerts a first-order control on the export of both POC_bio and POC_petro from the CLP to the Yellow River, resulting in more than 90% of the annual POC exported during the monsoon season. Around one third of annual POC erosional flux was transported during a storm event period, highlighting the important role of extreme events in POC export in this large river. © 2020 John Wiley & Sons, Ltd.