Suspended Particulate Matter Samples Research Articles

Relevance of using the non-reactive geochemical signature in sediment core to estimate historical tributary contributions

Fluvial suspended particulate matter (SPM) fluxes transport large amounts of contaminants that can affect water quality and river ecosystems. To better manage these inputs in river systems, it is essential to identify SPM and sediment sources. Many studies have applied a fingerprinting method based on using metals integrated into a numerical mixing model to estimate source contributions in a watershed. Most fingerprinting studies use contemporary SPM to trace historical inputs, whereas their metal concentrations were modified over time due to anthropogenic inputs. Moreover, total concentrations of these properties are subject to change due to diagenetic processes occurring in stored sediments. The aim of this study was to assess the relevance of using the non-reactive fraction of metals (i.e. metals and metalloids) in fingerprinting studies to estimate the historical contributions of SPM tributary inputs in a sediment core. To assess metal concentrations in the ‘conservative’ (i.e. non-reactive) fraction, SPM (samples of sources) and sediment core layers (targeted sediments) were subjected to total mineralization and soft extraction, and the non-reactive fraction was obtained by calculating the difference between the two extractions. This approach was applied on a sediment core from the Upper Rhône River (France), using geochemical signature in contemporary SPM of three major tributaries. We showed that the non-reactive fraction retains a higher number of metals in the range test for the deepest layers, which are characterized by significant anthropogenic inputs. Through apportionment modelling using Monte Carlo simulation, we demonstrated that the tributary contributions computed using the non-reactive fraction are more consistent with historical flood and water flow data and have lower uncertainties than with the total fraction. Working with the non-reactive fraction made it possible to decipher historical inputs of SPM using contemporary SPM samples. This approach enables robust identification of sub-catchment areas liable to provide large quantities of SPM. The non-reactive fraction can be used in a variety of environmental conditions and at various spatial and temporal scales to provide a robust quantification of sediment sources.

Energy dispersive X‐ray fluorescence methodology and analysis of suspended particulate matter in seawater for trace element compositions and an intercomparison with high‐resolution inductively coupled plasma‐mass spectrometry

AbstractA modification of energy dispersive X‐ray fluorescence (ED‐XRF) for analysis of trace element concentrations in suspended particulate matter (SPM) in seawater and intercomparison with high‐resolution inductively coupled plasma‐mass spectrometry (HR ICP‐MS) is presented. Approximately 250 SPM samples were collected on polycarbonate track‐etched filters in the Indian Ocean during the U.S. CLIVAR/CO2 Repeat Hydrography meridional section I09N cruise in 2007. Samples were first analyzed by ED‐XRF, a nondestructive technique, for Al, P, Ti, Mn, Fe, Ni, Cu, and Zn and subsequently digested and quantified by HR ICP‐MS, creating two blind, basin‐scale data sets used for a paired statistical comparison. Our results found (1) ED‐XRF analysis using thin‐film principles can quantify the elemental composition of SPM at nanomolar concentrations found in the open ocean; (2) there was excellent agreement between ED‐XRF and HR ICP‐MS analyses for Al, Fe, and Mn and good agreement for P and Ti; (3) analytical differences were the largest for Cu, Ni, and Zn; (4) HR ICP‐MS methods have lower detection limits for most elements when compared to the ED‐XRF; (5) ED‐XRF analysis has a closer agreement to reported values for the NIST SRM 2783 standard and lower relative standard deviations when compared to the HR ICP‐MS. We recommend continued refinement of nondestructive ED‐XRF methods as this would allow for the easy exchange of filtered samples between lab groups for intercalibration and intercomparison of basin‐scale hydrographic cruises and archival for future analysis.

Polycyclic aromatic hydrocarbons (PAHs) in the non-bleached and bleached corals and their ambient environment: The role of suspended particulate matter, mucus, and positive matrix factorization model for identifying contributions to the carcinogenicity of PAH sources

This study investigates levels of polycyclic aromatic hydrocarbons (PAHs) in the corals (tissue, skeleton, zooxanthellae, mucus) and their ambient environment (surface sediment, seawater, suspended particulate matter (SPM)), with a special focus on SPM and mucus. The Σ37PAH concentrations ranged from 89 to 206 ng g−1 dw in SPM, 52 to 116.1 ng g−1 dw in the sediment and from 18.6 to 91.9 ng L−1 in the seawater. Among the coral components, mucus contained the highest PAH loadings reaching up to 369.2 ng g−1 dw. Coral morphology and pollution of their ambient environment were identified as the main factors affecting the PAH bioaccumulation. Massive corals T. reinformes and P. compressa living in heavier polluted sites accumulated the highest PAH concentrations. Diagnostic ratios provided inconsistent source apportionment results, but positive matrix factorization (PMF) analysis identified gasoline/diesel (vehicle) emission (F1), oil spills (F2), coal (F3), and wood (F4) combustion as the main PAHs sources in the study area. Contribution to carcinogenic potencies of PAHs in sediment samples decreased in the following order: F1 > F2 > F3. Factor F4 did not affect the carcinogenic properties of the surface sediment samples but was found to contribute significantly to the TEQBaP values of the SPM samples. The results of this study indicate a direct interaction between SPM and the coral mucus and imply that SPM plays an important role in the pollution transfer and bioaccumulation processes in corals.

Terrestrial inputs govern spatial distribution of polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB) in an Arctic fjord system (Isfjorden, Svalbard).

Considerable amounts of previously deposited persistent organic pollutants (POPs) are stored in the Arctic cryosphere. Transport of freshwater and terrestrial material to the Arctic Ocean is increasing due to ongoing climate change and the impact this has on POPs in marine receiving systems is unknown This study has investigated how secondary sources of POPs from land influence the occurrence and fate of POPs in an Arctic coastal marine system. Passive sampling of water and sampling of riverine suspended particulate matter (SPM) and marine sediments for analysis of polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB) was carried out in rivers and their receiving fjords in Isfjorden system in Svalbard. Riverine SPM had low contaminant concentrations (<level of detection-28pg/g dw ΣPCB14, 16-100pg/g dw HCB) compared to outer marine sediments 630-880pg/g dw ΣPCB14, 530-770pg/g dw HCB). There was a strong spatial gradient in sediment PCB and HCB concentrations with lowest concentrations in river estuaries and in front of marine-terminating glaciers and increasing concentrations toward the outer fjord. This suggests that rather than leading to increased concentrations, inputs of SPM from land lead to a dilution of contaminant concentrations in nearshore sediments. Preliminary estimates of SPM:water activity ratios suggest that terrestrial particles (with low contaminant concentrations) may have the potential to act as sorbents of dissolved contaminants in the coastal water column, with implications for bioavailability of POPs to the marine food web. There is concern that ongoing increases in fluxes of freshwater, sediments and associated terrestrial material (including contaminants) from land to the Arctic Ocean will lead to increased mobilization and transport of POPs to coastal ecosystems. However, the results of this study indicate that on Svalbard, inputs from land may in fact have the opposite effect, leading to reduced concentrations in coastal sediments and waters.

Multi-matrix approach reveals the distribution of pesticides in a multipurpose protected area from the Atlantic Rainforest: potential risk for aquatic biota and human health?

The Atlantic Rainforest is among the main biodiversity hotspots in the world, the Yabotí Biosphere Reserve (YBR) being one of the most important remaining areas. Agriculture practices could lead to intensive usage of pesticides resulting in a risk to the environment and human health. Water, suspended particulate matter (SPM), sediment, and fish (Andromakhe paris and Andromakhe saguazu) samples were collected from four streams with different degrees of protection of the YBR in two periods in order to assess the distribution of 18 organochlorine pesticides. Legacy and current-use pesticides were found in the different environmental matrices of the stream headwaters in non-anthropized areas within the buffer zone that drains the intangible area. A similar occurrence pattern of pesticides was found in all matrices. Levels of DDTs (<3.63 ng/L) and endosulfans (<21.8 ng/L) in surface water were above international guidelines for the protection of aquatic life in several streams for both sampling periods. HCHs, DDTs, endosulfans, and chlorpyrifos were detected in SPM and sediments from three streams, while γ-HCH (<60.3 ng/g lipid weight), chlorpyrifos (<698 ng/g lw), p,p´-DDD (<367 ng/g lw), and α-endosulfans (<209 ng/g lw) were detected in fish muscle in several streams. Chlorpyrifos and endosulfans were associated with current use, while DDx/DDT ratios suggested an old use. The concentration of pesticides found would not represent a risk to human health; however, it highlights the need to establish better regulation and action guidelines to reduce the anthropogenic effect on natural reserves.

Latitudinal changes in the trophic structure of benthic coastal food webs along the Antarctic Peninsula

Stable isotopes of C and N have been used to assess the effect of the duration of the sea ice season on the structure of benthic, Antarctic coastal food webs. Samples of suspended particulate organic matter, macroalgae and macroinvertebrates were collected at five subtidal rocky sites across a latitudinal gradient along the western Antarctic Peninsula and among the South Shetland Islands. We tested the hypotheses that trophic positions of omnivores decrease, and food web structure becomes more redundant at higher latitudes. A latitudinal shift in the isotope baseline was detected for both δ13C and δ15N, but the trophic positions of macroinvertebrates and their relative positions along the δ13C axis and were basically constant across sites, even after rescaling stable isotope ratios to account for shifts in the baseline. Although the northernmost and southernmost study sites differed significantly in most of the metrics of the food web structure, changes with latitude and the duration of the sea ice season were non-monotonic. Highly productive phytoplankton blooms during the ice-free season at Esperanza Bay and Rothera Point may explain the observed pattern, as they result in a massive supply of planktonic organic matter to the detritus bank in the seabed and, hence, shorten the C range and increase trophic redundancy. If this hypothesis is correct, the intensity of the summer phytoplankton bloom can be as relevant for the structure of the benthic marine food web as the duration of the sea ice season.

Distribution, fractionation and sources of rare earth elements in suspended particulate matter in a tropical agricultural catchment, northeast Thailand

Forty-eight suspended particulate matter (SPM) samples were collected from the Mun River, northeast Thailand and its junction with the Mekong River, to investigate the relationship between the distribution of rare earth elements (REE) in SPM and the soils in the watershed. The total REE contents (∑REE) in SPM in the Mun River ranged from 78.5 to 377.8 mg/kg with the average of 189.3 mg/kg, which was lower than ∑REE of 222.3 mg/kg at the Mekong River (one sample at junction). The Post Archean Australia Shale (PAAS)-normalized ratios of light REE (LREE), middle REE (MREE) and heavy REE (HREE) were averaged to 1.0, 1.3 and 1.0, which showed a clear enrichment in MREE. In short, along the Mun River, the REE contents in SPM were decreasing, and the PAAS-normalized patterns of REE showed gradually flat. The REE content in SPM and soils are highest in the upper catchment, indicating that soil/bedrock is the most important source of REE in SPM. Additionally, the positive Eu anomaly was enhanced by the higher Ca content in SPM (R = 0.45), which may be caused by more feldspars or carbonates with Ca and Eu substituting Ca. The results present the REE behaviors of SPM in the Mun River and relationship between REE in SPM and soil/bedrock, the findings may support the other studies in catchment weathering.

Organophosphate esters in water, suspended particulate matter (SPM) and sediments of the Minjiang River, China

As organic pollutants of emerging concern, organophosphate esters (OPEs) have shown toxicity to organisms after entering the water environment. However, research on OPEs in freshwater in Southwest China is very limited. The levels, distribution and partitioning behavior of OPEs in the Minjiang River and their influencing factors is still unknown. In this study, six OPEs, tri-n-butyl phosphate (TnBP), tri(2-chloroethyl)-phosphate (TCEP), trichloropropyl phosphate (TCPP), triphenyl phosphate (TPhP), tributoxyethyl phosphate (TBEP), and tris(2-ethylhexyl)-phosphate (TEHP), were determined in surface water, suspended particle matter (SPM) and sediments of the Minjiang River. The results showed that the average concentrations of Σ6OPEs in surface water, SPM and sediments of the Minjiang River were 199.32 ± 124.95 ng/L, 38463.79 ± 45641.89 ng/g dry weight (dw) and 76.45 ± 28.00 ng/g dw, respectively. High concentrations of OPEs were detected in SPM samples, indicating that more attention should be paid to pollution in SPM. It is worth noting that the variation trend of OPEs in SPM was almost opposite to that in water but basically similar to that in sediment. The proportions of alkyl OPEs in Σ6OPEs increased from surface water to SPM and sediments. Alkyl OPEs were the main pollutants in SPM (10.44%–80.88% of Σ6OPEs, mean of 54.52%) and sediments (59.08%–81.30% of Σ6OPEs, mean of 68.91%), whereas chlorinated OPEs were the most abundant components in surface water (43.16%–75.99% of Σ6OPEs, mean of 55.50%). The water-sediment partition coefficient (logKOC) of OPEs was 4.97–7.58, while the water-SPM partition coefficient was 6.71–10.00. No significant correlations were found between logKOW and logKOC. KOW was not the main factor affecting the distribution of OPEs in the Minjiang River, China.

PCBs, HCB and PAHs in the seawater of Arctic fjords – Distribution, sources and risk assessment

In the present study, we examine contamination with PCBs, HCB and PAHs in the seawater of Arctic fjords (Hornsund, Kongsfjorden and Adventfjorden) which differ in environmental conditions and are particularly sensitive to climate change. We also investigate how the melting glaciers and ocean currents may affect the distribution and fate of target compounds in the seawater column in the fjords. The ∑7 PCB, HCB and ∑12 PAH concentrations in seawater ranged from, respectively: 0.002 to 41.2 ng/L; from LOQ to 233 ng/L; and from 0.196 to 311 ng/L. The research indicates that the concentrations of contaminants detected in Arctic fjords depend on the physicochemical properties of these compounds, local human activity and occurrence of glacier meltwaters. Detected HCB and PAH concentrations in most of the seawater samples were at levels classified as harmless, however in 30 out of 80 analysed suspended particulate matter samples some compounds were present at toxic levels.

Viability and stress state of bacteria associated with primary production or zooplankton-derived suspended particulate matter in summer along a transect in Baffin Bay (Arctic Ocean)

In the framework of the GreenEdge Project (whose the general objective is to understand the dynamic of the phytoplankton spring bloom in Arctic Ocean), lipid composition and viability and stress state of bacteria were monitored in sea ice and suspended particulate matter (SPM) samples collected in 2016 along a transect from sea ice to open water in Baffin Bay (Arctic Ocean). Lipid analyses confirmed the dominance of diatoms in the bottommost layer of ice and suggested (i) the presence of a strong proportion of micro-zooplankton in SPM samples collected at the western ice covered St 403 and St 409 and (ii) a high proportion of macro-zooplankton (copepods) in SPM samples collected at the eastern ice covered St 413 and open water St 418. The use of the propidium monoazide (PMA) method allowed to show a high bacterial mortality in sea ice and in SPM material collected in shallower waters at St 409 and St 418. This mortality was attributed to the release of bactericidal free fatty acids by sympagic diatoms under the effect of light stress. A strong cis-trans isomerization of bacterial MUFAs was observed in the deeper SPM samples collected at the St 403 and St 409. It was attributed to the ingestion of bacteria stressed by salinity in brine channels of ice by sympagic bacterivorous microzooplankton (ciliates) incorporating trans fatty acids of their preys before to be released in the water column during melting. The high trans/cis ratios also observed in SPM samples collected in the shallower waters at St 413 and St 418 suggest the presence of positively or neutrally buoyant extracellular polymeric substances (EPS)-rich particles retained in sea ice and discharged (with bacteria stressed by salinity) in seawater after the initial release of algal biomass. Such EPS particles, which are generally considered as ideal vectors for bacterial horizontal distribution in the Arctic, appeared to contain a high proportion of dead and non-growing bacteria.

Under the influence of regulations: spatio-temporal trends of the UV filter 2-Ethylhexyl-4-methoxycinnamate (EHMC) in German rivers

BackgroundGlobally, 2-Ethylhexyl-4-methoxycinnamate (EHMC) is one of the most commonly used UV filters in sunscreen and personal care products. Due to its widespread usage, the occurrence of EHMC in the aquatic environment has frequently been documented. In the EU, EHMC is listed under the European Community Rolling Action Plan (CoRAP) as suspected to be persistent, bioaccumulative, and toxic (PBT) and as a potential endocrine disruptor. It was included in the first watch list under the Water Framework Directive (WFD) referring to a sediment PNEC of 200 µg/kg dry weight (dw). In the light of the ongoing substance evaluation to refine the environmental risk assessment, the objective of this study was to obtain spatio-temporal trends for EHMC in freshwater.We analyzed samples of suspended particulate matter (SPM) retrieved from the German environmental specimen bank (ESB). The samples covered 13 sampling sites from major German rivers, including Rhine, Elbe, and Danube, and have been collected since mid-2000s.ResultsOur results show decreasing concentrations of EHMC in annual SPM samples during the studied period. In the mid-2000s, the levels for EHMC ranged between 3.3 and 72 ng/g dw. The highest burden could be found in the Rhine tributary Saar. In 2017, we observed a maximum concentration ten times lower (7.9 ng/g dw in samples from the Saar). In 62% of all samples taken in 2017, concentrations were even below the limit of quantification (LOQ) of 2.7 ng/g dw.ConclusionsThe results indicate a general declining discharge of EHMC into German rivers within the last 15 years and correspond to the market data. Although the measured levels are below the predicted no-effect level (PNEC) in sediment, further research should identify local and seasonal level of exposure, e.g., at highly frequented bathing waters especially in lakes. In addition, possible substitutes as well as their potentially synergistic effects together with other UV filters should be investigated.

Carbon and nitrogen stable isotopes of copepods in a tidal estuarine system in Maryland, USA

The carbon and nitrogen stable isotope ratios of copepods, particularly Acartia tonsa and suspended particulate organic matter (SPOM) samples, collected seasonally (2014 to 2017) from 13 sites in the tidal estuaries of Maryland were analyzed. We hypothesized that copepods at sites close to the mouths of lagoon tributaries have more depleted δ13C than copepods at sites near the inlets, and that variations in the δ13C values of copepods mirror that of the SPOM. Copepod δ13C values ranged from −27.8‰ to −19.4‰, and that of SPOM from −26.8 to −20.3‰. Mean copepod δ13C value (−21.8‰±0.4) at a site close to the ocean was the highest, whereas the lowest value (−24.4‰±0.5) occurred at a site located at the mouth of St. Martin River. δ15N copepod values varied from 2.9‰ to 13.0‰ (mean=9.2‰±0.1); that of SPOM was −0.58 to 10.51‰ (mean=5.7‰±0.2). Reduction in the δ15N mean values from a site near the Ocean City inlet (10.2±0.4‰) to a site close to the tributaries (8.5±0.6‰) suggests that copepods at the site near Ocean City inlet likely fed on food items that contained more marine phytoplankton with enriched δ15N and heterotrophic protists, than copepods at a site near the river mouth. The highest (−21.9‰±0.4) and lowest (−25.8‰±0.3) mean copepod δ13C values were observed in summer 2015 and winter 2017, whereas the highest (10.8‰±0.2) and lowest (7.1‰±0.7) mean copepod δ15N values were recorded in winter and fall 2016, respectively. δ15N enrichment between copepods and SPOM ranged from 1.0‰ to 8.9‰ (mean: 3.4‰). The highest enrichment observed in February 2016 stemmed from a reduction in SPOM δ15N values, after a major storm event, which was unaccompanied by a decrease in Acartiaδ15N. Copepod and SPOM δ13C and δ15N values, displayed similar spatial patterns and were positively correlated; enrichment at sites near the ocean and depletion near the river mouth indicating that SPOM composition influenced copepods diets in the lagoons.

Levels of dioxins and dioxin-like polychlorinated biphenyls in seawater from the Hornsund fjord (SW Svalbard)

Knowledge of contaminant distribution is important, particularly in the vulnerable first results about the occurrence of seventeen polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans and twelve dioxin-like polychlorinated biphenyls in arctic fjord seawater are reported. The contaminants were measured in 10 samples of suspended particulate matter collected in Hornsund (Svalbard). The ∑PCDD/F and ∑dl-PCB concentrations ranged from 0.066 to 231.47 pg/L and from 2.43 to 46.43 pg/L respectively. In terms of total PCDD/Fs, in general highly chlorinated PCDFs constituted the most significant fraction. Among dl-PCB compounds, PCB118 was the dominant congener. The toxicity equivalent for the samples ranged from 0.0008 to 1.90 pg I-TEQ/L for ∑PCDD/Fs, while for ∑dl-PCB it ranged from 0.0002 to 0.024 pg WHO05-TEQ/L. High concentrations of dioxins and dl-PCBs in some samples indicated that those contaminants could pose a threat to marine biota.

Particulate Mercury and Particulate Organic Matter in the Itenez Basin (Bolivia)

In rivers and other freshwater bodies, the presence of mercury can be due to direct contamination by anthropic activities such as gold mining. However, it can also be attributed to atmospheric deposition and erosion, runoff, or lixiviation from surrounding soils. In the case of the Amazon rainforest, high mercury contents have been reported for litter and topsoil, which could affect the mercury concentrations in water bodies. Samples of suspended particulate matter were obtained from a transect of the Itenez River, associated lakes, and some of its tributaries. The aim was to obtain information on particulate mercury’s origin in the study area and determine the relationship between particulate mercury and particulate organic carbon. The concentration of mercury, organic matter, and the C:N ratio of the suspended matter was determined. The concentration of particulate mercury by water volume depended on changes in suspended matter loads, which in turn were mostly affected by the nature of the watershed or sediment resuspension. The observed values for the percentage of organic matter and the C:N ratio suggest that most of the mercury content in rivers and lakes originated from soils. A positive correlation was found between mercury concentration by weight of particulate matter and organic carbon content in particles. This correlation might be due to the direct binding of mercury to organic matter through functional groups like thiols or to an indirect effect of oxyhydroxides that can adsorb mercury and are associated with organic matter.

Polychlorinated biphenyls and organochlorine pesticides in water and sediment from Volturno River, Southern Italy: occurrence, distribution and risk assessment

BackgroundTo assess the Volturno River pollution and its environmental impact on the Tyrrhenian Sea (Central Mediterranean Sea) caused by Polychlorinated biphenyls (PCBs) and Organochlorine pesticides (OCPs), 32 PCBs and aldrin, α-BHC, β-BHC, δ-BHC, γ-BHC (lindane), 4,4′- DDD, 4,4′-DDE, 4,4′-DDT, dieldrin, endosulfan I, endosulfan II, endosulfan sulphate, endrin, heptachlor, heptachlor epoxide (isomer B) and methoxychlor have been selected and were analyzed in three different phases: dissolved phase (DP), suspended particulate matter (SPM) and sediments. PCBs and OCPs were extracted using an SPE column for the DP and glass fiber filter for SPM and sediment samples. Cleaned extracts were analyzed by gas chromatography with electron capture detector (ECD) and mass spectrometry (MS) detector for PCBs and OCPs, respectively.ResultsPollutants discharges of PCBs and OCPs into the sea were calculated in about 106.9 kg year−1 (87.1 kg year−1 of PCBs and 19.7 kg year−1 of OCPs), showing that this river could be a major source of PCBs and OCPs pollution to the Central Mediterranean Sea. Total concentrations of PCBs ranged from 4.1 to 48.0 ng L−1 in water (sum of DP and SPM) and from 4.3 to 64.3 ng g−1 in sediment samples. The concentrations of total organochlorine pesticides (OCPs) obtained in water (sum of DP and SPM) ranged from 0.93 to 8.66 ng L−1 and from 0.52 to 9.89 ng g−1 in sediment samples. Principal component analysis shows that all PCB compounds are more likely to come from surface runoff than an atmospheric deposition.ConclusionThe data show that higher levels of PCBs and OCPs were found in sediment samples than in DP and SPM samples, which are an indication of no fresh inputs of these compounds. Based on our results, unintentionally produced PCBs by industrial processes (and other processes) were considered to be the main sources of PCBs in Volturno River and Estuary sediments. Considering the Sediment Quality Guidelines (SQGs), the Ecological Risk Index (ERI), the Risk Quotient (RQ) and the USEPA Environmental Quality Standards (EQS), the Volturno River and its Estuary would be considered an area in which the integrity is possibly at risk.

Aquatic suspended particulate matter as source of eDNA for fish metabarcoding

The use of environmental DNA (eDNA) for monitoring aquatic macrofauna allows the non-invasive species determination and measurement of their DNA abundance and typically involves the analysis of eDNA captured from water samples. In this proof-of-concept study, we focused on the novel use of eDNA extracted from archived suspended particulate matter (SPM) for identifying fish species using metabarcoding, which benefits from the prospect of retrospective monitoring and also analysis of fish communities through time. We used archived SPM samples of the German Environmental Specimen Bank (ESB), which were collected using sedimentation traps from different riverine points in Germany. Environmental DNA was extracted from nine SPM samples differing in location, organic content, and porosity (among other factors) using four different methods for the isolation of high-quality DNA. Application of the PowerSoil DNA Isolation Kit with an overnight incubation in lysis buffer, resulted in DNA extraction with the highest purity and eDNA metabarcoding of these eDNA fragments was used to detect a total of 29 fish taxa among the analyzed samples. Here we demonstrated for the first time that SPM is a promising source of eDNA for metabarcoding analysis, which could provide valuable retrospective information (when using archived SPM) for fish monitoring, complementing the currently used approaches.

Temporal and spatial variability of the suspended particulate matter in the Gdansk Deep and Eastern Gotland Basin

The work was carried out in the south-eastern part of the Baltic Sea on the meridional section along the Russian–Polish border during 2015–2018 using the CTD-sounding. The suspended particulate matter samples were taken with the use of ultrafiltration of sea water (0.4 micron filters). The research was focused on identifying the temporal and spatial variability of suspended particulate matter distribution after a series of inflows of the North Sea waters in 2014–2016. The vertical structure of the suspended particulate matter distribution in the south-eastern Baltic, both on a seasonal and interannual scale, contains the main features common for all marine basins, namely increased concentrations of SPM at the sea surface and bottom and an intermediate layer of minimum concentrations located at a depth of 50–70 m. Seasonal fluctuations in the SPM concentration are very significant and are mainly due to the seasonal variation of bioproduction in the surface layer of the sea and the flow of rivers. The confirmation of the barrier role of density boundaries (thermocline and halocline) in sedimentation and geochemical processes has not been obtained.

Dynamics of Hg and MeHg in the Madeira River basin (Western Amazon) before and after impoundment of a run-of-river hydroelectric dam

The impact of a hydroelectric run-of-river (RoR) dam construction on the dynamics of total mercury (THg) and methylmercury (MeHg) is of interest to the environment and health of human and wild life. We monitored (May 2010 to October 2018) THg and MeHg in the waters and in the suspended particulate matter (SPM) of the Madeira River and its tributaries (before and after dam construction) to evaluate changes upstream and downstream from the Santo Antonio Hydroelectric Dam (SAHD). We collected 2826 samples of water and SPM at sampling stations upstream (UPMD-01, UPMD-02 and UPMD-03) and downstream the Madeira River (DWMD-04, DWMD-05 and DWMD-06), and Tributaries upstream (Branco River, Jaci-Parana River, Jatuarana-I Igarapé, Contra River, Caripunas Igarapé, Ceara Igarapé, and Teotonio Igarapé) and downstream (Jatuarana-II Igarapé and Belmont Igarapé) from the SAHD and monitored water and the total load of SPM. SPM was significantly higher in the Madeira River (median: 178.63 mg.L−1) than in upstream and downstream tributaries (median: 15.30 mg.L−1); however, the THg and MeHg concentrations were significantly higher in the tributaries (median: 161.14 ng g−1 and 9.03 ng g−1, respectively) than in the mainstream Madeira River (median = 57.06 ng g−1 and 1.63 ng g−1, respectively). THg concentration in the water was significantly higher in the mainstream Madeira River (median = 6.51 ng.L−1) than in the tributaries (median = 2.57 ng.L−1). However, the percentage of methylation in the tributaries (median = 4.9%) was 4-times higher than in the Madeira River (median: 1.3%). The significantly higher MeHg percentages in the tributaries may indicate natural (hydro-bio-geochemical factors) still predominant in this changing landscape of the Western Amazon. So far, the data suggest that this RoR has not yet impacted the THg and MeHg concentrations.

Correlation between the ratio of 5-methyl hexamethylated to pentamethylated branched GDGTs (HP5) and water depth reflects redox variations in stratified lakes

Branched glycerol dialkyl glycerol tetraethers (brGDGTs) are potentially valuable biomarkers for paleoclimatic and paleoenvironmental studies. However, multiple factors controlling their variations in lake sediments hamper the widespread application of brGDGT-based proxies. Here we investigate brGDGTs in water column suspended particulate matter (SPM) and surface sediments in a series of lakes with a wide range of depths from three main volcanic fields of northeastern China. The brGDGT distribution patterns from SPM and surface sediments of these lakes differ greatly from those of surrounding soils, indicating a predominant aquatic origin for brGDGTs. We find that the ratio of 5-methyl hexamethylated and pentamethylated brGDGTs with no cyclopentane rings (IIIa/(IIa + IIIa); designated as HP5) is strongly correlated with water depth. Re-examination of published brGDGT data from SPM samples in redox-stratified Lake Lugano reveals similar relationships, whereas such correlations are much weaker in Lake Superior which does not have an anoxic hypolimnion. Importantly, we find that there is strong correlation between HP5 and dissolved oxygen in water column of the redox-stratified lakes, suggesting that the observed apparent HP5–water depth correlation may be primarily attributed to depth-progressive shifts in the brGDGT-producing bacterial communities with different redox requirements (aerobic, facultative anaerobic, and anaerobic bacteria). Notably, brGDGT methylation indices (MBTʹ5ME and MBTʹ6ME) of surface sediments display poor correlations with air temperatures in our study lakes, calling for caution in applying MBTʹ5ME and MBTʹ6ME as temperature proxies in these lakes.

Connecting land use−land cover and precipitation with organic matter biogeochemistry in a tropical river–estuary system of western peninsular India

Organic matter (OM) composition changed due to land use ─ land cover (LULC) and hydrology modification, has distinctive linkage towards sustainable environment management in tropical river systems. It is crucial in small river systems, which experience delay of freshwater flow to the estuaries due to headwater damming, also LULC alteration along the entire basin. In order to understand this fundamental linkage in tropical Zuari river-estuary (ZRE), we analyzed multi-proxy data of organic carbon to total nitrogen ratio (Corg/N), stable organic carbon isotope (δ13Corg) and lignin phenols measured in seasonally collected suspended particulate matter (SPM) and sediment samples. Results highlighted about moderate seasonality of OM tracers, with a significant effect of LULC alteration, which nevertheless a striking feature in monsoon-fed river-estuaries of peninsular India. Particulate Corg export from ZRE estimated to be 20 × 103 kg yr−1, was much lower as compared to tropical river-estuary systems elsewhere. OM fraction from vascular plant (mangroves) contributed to SPM and sediment was 15% and 40%, respectively, calculated using a Bayesian mixing calculation through Stable isotope analysis in R (SIAR). Presence of mudflat LULC in the estuarine region notably caused 20% decrease in Corg and 60% increase in lignin phenol (Λ8) as compared to their limits in upstream. This is although mudflat accounts only 3% of ZRE catchment. The degree of shifts in OM tracers highlights towards efficient entrapment, transformation and/or utilization of riverine OM in the mudflats of ZRE. Accelerated human induced LULC dampens the seasonality of OM characteristics and flow is highlighted through this study, which is essential towards sustainable environmental management practice in small rivers of India and World.