Sediment Dry Weight Research Articles

Partitioning behavior, source identification, and risk assessment of perfluorinated compounds in an industry-influenced river

BackgroundThe widespread application of perfluorinated compounds (PFCs) makes them ubiquitously distributed in the environment. Investigation of contamination profiles, distribution, possible sources and risks of PFCs in Liaohe River, an industry-influenced river in northeast China was conducted in the present study.ResultsThe total PFCs concentrations (∑PFCs) were in the range 0.38–127.88 ng/L (average value of 36.41 ng/L) in water and 1.72–10.44 ng/g dry weight (average of 4.99 ng/g) in sediment. Perfluorooctanoic acid (PFOA) was the dominant individual in water and sediment phases, in the range 0.38–73.94 ng/L in water and below detection limit (BDL) to 7.88 ng/g dw in the sediments. The organic carbon normalized partition coefficients (Koc) ranged from 2.46 L/kg (PFHxA) to 4.29 L/kg (PFUnDA). The average Koc values for perfluorocarboxylic acids (PFCAs) increased by 0.13–0.62 log unit with each increasing CF2 moiety, and the Koc values were lower than perfluoroalkyl sulfonates (PFASs). The sources of PFCs identified from diagnostic ratios suggested that the contaminants were mainly from the emission of manufacturing processes and precursors degradation. Result from risk assessment indicated that the immediate health impact through intaking water was negligible, but the levels of PFOA in surface water might cause effects on aquatic ecosystem. The mass inventories of ∑PFCs and PFOA were estimated to be 328.74 t and 103.43 t in the study area, respectively, suggesting that the sediment in Liaohe River may act as a potential PFCs source to the surrounding areas.ConclusionThis study demonstrated that PFCs were widely presented in the water and sediments of Liaohe River. In general, PFCAs had higher concentrations and detection frequency than PFSAs, and PFCAs with short carbon chains had much higher detection frequencies than long-carbon chain compounds in water. Among all PFC homologues, the average Koc increased with the increased carbon chain. Koc values were higher for PFSAs than PFCAs. The risk assessment suggested that PFOA in water may exert adverse effect on the aquatic ecosystem. Liaohe River was likely acting as a PFCs source to the surrounding area.

The spatial distribution of phytoplankton pigments in the surface sediments of the Kongsfjorden and Krossfjorden ecosystem of Svalbard, Arctic

Kongsfjorden–Krossfjorden twin fjord ecosystem in Svalbard (Arctic), is facing enhanced warm Atlantic water intrusion from ocean as well as intensified melting from glaciers. It is an interesting ecosystem to study phytoplankton productivity under the two opposing processes. For phytoplankton productivity, pigments are used as potential photosynthetic biomass indicators and taxonomic biomarkers. However, due to labile nature of pigments, degradation — preservation distribution must be investigated to form essential framework for biomarker studies. With this motivation, we have undertaken the present work to study the spatial distribution of surface sedimentary pigments in the twin-fjord ecosystem. The pigments were analysed using high-performance liquid chromatography coupled with diode array detector. A total of fifteen pigments were identified, which belonged to different classes — chlorophylls, pheopigments and carotenoids. Chlorophyll-a and pheophorbide-a were major pigments with concentration up to 700–800 ng g−1 dry weight of sediment. Among carotenoids, fucoxanthin, diatoxanthin and prasinoxanthin were abundant with maximum concentration recorded up to 400–600 ng g−1 dry weight. The distribution of the pigments varied significantly between the two fjords as well as in different regions of the fjord. Most of the pigments were significantly high in their concentration at Krossfjorden stations. Within Kongsfjorden, outer region showed higher concentration of pigments than inner. However, preservation was lesser for the outer fjord pigments than inner as confirmed by various pigment indices. Further, the overall distribution of phytoplankton communities derived from taxonomic biomarker pigments in Kongsfjorden–Krossfjorden sediments, was coherent with that of water during spring and summer. The distribution was dominated by diatoms, dinoflagellates, prasinophytes and prymnesiophytes. The surface sedimentary pigments were found capable of providing information about phytoplankton biomass and composition under environmental conditions existing in the region.

The impact of improper solid waste management to plastic pollution in Indonesian coast and marine environment.

Plastic pollution has become a major concern in Indonesian coast and marine environment today. It occurs because 14% of the solid waste (SW) components in this country is plastic, and the SW management (SWM) infrastructure and services are still limited. The objectives of this article are to discuss the improper SWM and its impact to plastic pollution in Indonesia. Ten plastic pollution studies concerning macroplastics (MaP) and microplastics (MP) were described. These studies covered 5 regions, namely Java, East Nusa Tenggara, East Kalimantan, South Sulawesi, North and Southwest Sumatera. The highest MP abundance of 37,440-38,790 particles/kg dry weight (DW) sediment was found in Jakarta Bay, followed by Wonorejo Coast in Surabaya City (414-590 MP particles/kg DW sediment). The MP has entered the food chain through bivalves and fish. Therefore, the plastic pollution which is related to population density, and inadequacy of SWM, needs urgent solution.

Polybrominated diphenyl ethers and polychlorinated biphenyls in mangrove sediments of Shantou, China: Occurrence, profiles, depth-distribution, and risk assessment

Surface and columnar sediments were collected from four mangrove Wetlands in Shantou coastal areas of South China to investigate the level, distribution, possible sources and ecotoxicological risks of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs). Total concentration of 14 PBDEs (∑14PBDEs) and 41 PCBs (∑41PCBs) varied from 0.61 to 180 ng/g and 42–636 pg/g dry weight (dw) in surface sediments, respectively. The concentration of PBDEs was much higher than that of PCBs. Compared with other mangrove Wetlands around the world, PCBs levels in the studied area were relatively low, while the concentrations of PBDE were at higher level. Decabromodiphenyl ether (BDE-209) was the predominant PBDEs homologue in all sediment samples, indicating the extensive use of deca-BDE in this area. Penta-CBs and hexa-CBs were the main homologues of PCBs. Spatial variations showed that the concentration of PBDEs might be mainly affected by anthropogenic activities in specific sites of this region, whereas dry and wet deposition might be an important input source of PCBs in this area. Although accurate sediment chronology was not available, higher concentrations of PBDEs and PCBs were still found in some deeper sediment layers, suggesting that new input quantity tends to decrease with the increase of control. Risk assessment showed that penta-BDEs and deca-BDE may have potential negative ecological effects on the ecological of Shantou mangrove sediments, while the effects of PCBs can be neglected.

Microplastic prevalence in the beaches of Puducherry, India and its correlation with fishing and tourism/recreational activities.

The prevalence of microplastics in the sediments of six beaches of the Puducherry coast in India was studied and its correlation to fishing activities and recreational activities was analysed. On an average, 72.03 ± 19.16 microplastic particles/100 g dry weight of sediments is found to be the microplastic abundance in the study. A Strong positive correlation (Pearson's R = 0.92, p = 0.0103) between fishing activity and microplastic abundance and a weak correlation (Pearson's R = 0.04, p = 0.932) between microplastic abundance and recreational activities is found. Majority (65.12%) of the microplastics belongs to the size bracket of 300 μm-1 mm and only 34.88% were large microplastics (>1 mm). The Polymers of the microplastics were identified as Polypropylene, HDPE, LDPE, Polystyrene, Polyurethane etc. using Raman spectroscopy. Microplastic fragments comprise 56.32% of the total particles. In terms of colour of the microplastics, white (26.92%) is the most abundant.

Cross shelf transport of terrigenous organic matter in surface sediments from outer shelf to Okinawa Trough in East China Sea

Identification of sources and distribution of terrigenous organic matter (TOM) are significant to understand the carbon transport in East China Sea (ECS). However, sources of TOM buried in the ECS are diverse and complex, which are likely derived from the Changjiang River, Yellow River and/or small rivers from China mainland and Taiwan. In order to evaluate the fate of TOM offshore in the ECS, the study sampled 80 surface sediments from outer shelf-slope-Okinawa Trough (OT) region in the ECS. Both terrigenous and marine organic biomarkers were detected. The concentration (ng/g dry weight sediment) of terrigenous biomarkers including ƩC27 + C29 + C31 n-alkanes ranged from 12.2 to 990.9; while the content of marine biomarkers varied from 1.3 to 3891.2 for C37 alkenones, 2.6 to 922.6 for brassicasterol and 7.1 to 1535.8 for dinosterol. Bulk organic carbon and TOM distributions were controlled by the hydrodynamic conditions. The terrigenous and marine biomarker ratio (TMBR) (ƩC27 + C29 + C31 n-alkanes)/(ƩC27 + C29 + C31 n-alkanes + (brassicasterol + dinosterol +alkenones)) increased first and decreased from the outer shelf to OT spatially, showing the distribution pattern of relative proportion of TOM. Hotspots of significant deposition of TOM were observed in the ECS by δ13C and TMBR proxies that the mechanism was unclear yet. Binary model revealed higher percentage of TOM based on TMBR than δ13C for both slope (32.1% vs. 20.0%) and trough (23.1% vs. 15.2%) region. An underestimation of C4 vegetation contribution likely biased the bulk carbon model. Carbon preference index suggested a zonation distribution of TOM that outer shelf had different sources from the slope and OT attributed to cross shelf transport of terrigenous organic matter.

Occurrence and identification of microplastics in beach sediments from the Hauts-de-France region.

The present work was carried out to quantify microplastics (MP) from three sandy beaches along the Côte d'Opale coastline located in the Hauts-de-France region of northern France. Three different study sites located along the English Channel were investigated due to different levels of anthropopression and hydrodynamic conditions. Sediments were collected at three different tide lines: high tide line (HTL), middle of the intertidal zone (IZ), and low tide line (LTL), to investigate the effects of tide line on microplastic contamination. Particles and fibers were counted and colors were recorded; polymer identification was then performed using pyrolysis-gas chromatography-mass spectrometry (Py-GC/MS). Particle and fiber abundances ranged from 23.4 ± 18.9 to 69.3 ± 30.6 items kg-1 dry weight sediment, with a trend towards fiber predominance, were observed. No difference in particle and fiber abundance was found between the different beaches and tide lines, except for Boulogne-sur-Mer, where the particle number was significantly different between tide lines. Major polymers identified were polyethylene (36.6%) and polypropylene (10.7%). This citizen science project provided preliminary data about the abundance and polymeric nature of MP along the Côte d'Opale coastline.

Concentration and distribution of per- and polyfluoroalkyl substances (PFAS) in the Asan Lake area of South Korea

Seasonal and spatial variations in per- and polyfluoroalkyl substances (PFAS) concentrations in different environmental media in the Asan Lake area of South Korea were investigated by measuring liquid chromatography-tandem mass spectrometry (LC–MS/MS). The mean concentrations of Σ16 PFAS in the different media were in the ranges of 20.7–98.2 pg/m3 in air, 17.7–467 ng/L in water, 0.04–15.0 ng/g dry weight (dw) in sediments, and not detected (n.d.)–12.9 ng/g dw in soils, and the mean concentrations of Σ19 PFAS in fish ranged from n.d. to 197 ng/g wet weight. The most frequently detected PFAS were perfluorooctanoic acid (PFOA) in air and soils, perfluoropentanoic acid (PFPeA) in water, and perfluorooctane sulfonate (PFOS) in sediment and fish. Long-chain PFAS species dominated over short-chain PFAS in most media samples except for the water phase. Sediment-water partition coefficients (log Kd) and bioaccumulation factors (log BAF) of PFAS were calculated using measured concentrations in water, sediments, and fish. Log Kd of PFAS tended to increase with increasing CF2 units of PFAS, and perfluorodecanoic acid (PFDA) and PFOS showed the highest log BAF value (> 3.0) in all fish species. These results indicate that longer-chain PFAS, especially PFOS, can be effectively accumulated in biota such as fish.

Occurrence and Environmental Distribution of 5 UV Filters During the Summer Season in Different Water Bodies

Organic UV filters are used worldwide in various personal care products as well as textiles, paints, plastic, food, and adhesives. They are main ingredients in sunscreen lotions that are used heavily by beachgoers in the summer season. There is thus an increasing concern regarding the fate of organic UV filters in the environment and their impact on living organisms. Many of the UV filters in use are hydrophobic and are expected to accumulate in the sediment phase in aquatic systems, but this has yet to be validated in situ. We targeted the UV filters benzophenone 3 (BP3), butyl methoxydibenzoylmethane (BMDBM), diethylhexyl butamido triazone (DBT), bis-ethylhexyloxyphenol methoxyphenyl triazine (BEMT), and methylene bis-benzotriazolyl tetramethylbutylphenol (MBBT) in a freshwater lake and in a coastal bay in order to understand their distribution during summer 2016. Further, we examined their environmental partitioning by collecting samples from the surface water, the sediment phase, and water surface microlayer (SML). We show for the first time the presence of DBT, BEMT, and MBBT in environmental matrices (water, SML, and sediment). Notably, these UV filters were detected at low amounts in surface waters with maximum concentrations of 9.9 ng/L for DBT, 18.4 ng/L for BEMT, and below detection limits for MBBT and somewhat higher concentrations in the SML, with maximum concentrations of 43.3 ng/L for DBT, 5625.4 ng/L for BEMT, and 45.6 ng/L for MBBT. These filters were detected at even greater concentrations in the sediments, with maximum concentrations of 652.6 ng/g for DBT, 115.0 ng/g for BEMT, and 75.2 ng/g for MBBT (dry weight sediment). We also performed controlled laboratory experiments to determine their partitioning behavior, and we verified the actual solubility of many of the filters. This will help in determining the environmental fate and finally lead to a better risk assessment of these compounds. Together, these results corroborate the hypothesis that hydrophobic UV filters accumulate in the sediment phase and highlight the importance of discerning whether these UV filters impact the benthic community and their potential for bioaccumulation.

Stabilization of hydrophobic organic contaminants in sediments by natural zeolites: bioavailability-based assessment of efficacy using equilibrium passive sampling

As natural zeolites have been widely used as cost-effective adsorbents for plant nutrients and heavy metals in sediments, it is worthwhile to verify the potential of natural zeolites for mixed-contaminant stabilization including hydrophobic organic contaminants (HOCs). The effectiveness of natural zeolite amendment in sediment on reducing the bioaccumulation of sediment-associated HOCs in V. philippinaram (Cb) was assessed. Then, the role of sediment pore water freely dissolved HOCs (Cfree) in Cb prediction was further identified and modeled. In this study, a bioavailability-based assessment of the HOC-stabilization efficacy of natural zeolites in maricultural sediments was performed using equilibrium passive sampling. V. philippinaram was adopted as a biological indicator for HOC bioaccumulation. Polydimethylsiloxane (PDMS) was used as a passive sampler for monitoring the concentration of the Cfree. The assumption that Cfree is a central mediator driving the bioaccumulation process of HOCs from the bulk sediment to the exposed organisms was validated by correlating the reductions in Cb and Cfree of the sediments amended with natural zeolites. Subsequently, a model based on this assumption was built and verified for the bioavailability-based assessment of the stabilization efficacy of natural zeolite amendment on sediment-associated HOCs. The results showed the bioaccumulations of four kinds of HOCs (including polycyclic aromatic hydrocarbons, polybrominated diphenyl ethers, pyrethroids, and organochlorine pesticides) in V. philippinaram were reduced by 7.3–38% after the natural zeolite amendment (10% dry weight in sediments), and the Cfree values measured with PDMS were reduced proportionally. It supported the assumption that Cfree is a central mediator driving the bioaccumulation process of HOCs. Kow of HOCs and two properties of sediment were found to be significantly correlated with the reductions of the Cfree values. Based on these findings, a model to predict the Cb values of PAHs and PBDEs in V. philippinaram was built. The model was then verified by a significant correlation between the predicted and measured values of Cb. The potential of natural zeolites for the stabilization of mixed-contaminants in sediments, including HOCs, was proved as notable reductions of Cb and Cfree of HOCs in the sediments amended by natural zeolite were observed. The results also suggested PDMS is a promising tool for predicting the bioaccumulation of sediment-associated HOCs in V. philippinaram and further for assessing the stabilization efficacy of natural zeolites in maricultural sediments. Modifying natural zeolites to further improve the effectiveness of HOC stabilization is warranted.

Occurrence, distribution and risk assessment of abused drugs and their metabolites in a typical urban river in north China

This study investigated the presence of 11 abused drugs and their metabolites, including amphetamine, methamphetamine (METH), ketamine, ephedrine (EPH), cocaine, benzoylecgonine, methadone, morphine, heroin, codeine, and methcathinone in the surface water and sediment samples of Beiyunhe River, a typical urban river flowing through Beijing, Tianjin, and Hebei provinces in North China. An analytical method of determining these abused drugs and their metabolites in water and sediment was developed and validated prior to sample collection in the study area. Results showed that METH and EPH were predominant in water and sediment samples. The total drug concentrations ranged from 26.6 to 183.0 ng/L in water and from 2.6 to 32.4 ng/g dry weight in sediment, and the drugs mainly originated from hospitals and sewage treatment plants. The average field-based sediment water distribution coefficients of abused drugs were calculated between 149.3 and 1214.0 L/kg and corrected by organic carbon. Quotient method was used to assess the risks. The findings revealed that these drugs and their metabolites at determined concentrations in water samples will not impair the aquatic ecosystem biologically, but their potential harmful effect on the function of the ecosystem and human health should not be overlooked.

Bioaccumulation and biomagnification of short-chain chlorinated paraffins in marine organisms from the Pearl River Estuary, South China

Short-chain chlorinated paraffins (SCCPs) are a series of new persistent organic pollutants, posing a risk of significant adverse effects to biota. Increasing attention has been paid to SCCP pollution in China as large amounts of chlorinated paraffin (CP) products containing SCCPs have been produced and used there. However, knowledge of the bioaccumulation of SCCPs in marine organisms from the Pearl River Estuary (PRE), Southern China, is still scarce. In this study, SCCP concentrations were measured in seawater, sediments, and marine organisms from the PRE. SCCP concentrations ranged from 180 to 460 ng/L in seawater, from 180 to 620 ng/g dry weight (dw) in sediments, and from 870 to 36,000 ng/g lipid weight (lw) in marine biota samples. C10–11 SCCPs were the predominant homologues in all the samples, with an average abundance of 68% in seawater, 57% in sediments, and 56–77% in marine organisms. However, chlorine patterns of SCCPs in seawater, sediments, and marine organisms were different. Cl8–10 SCCPs dominated in sediments, whereas Cl5–7 SCCPs were the predominant SCCP homologues in water and most organism species. The logarithm bioaccumulation factors (BAFs) of SCCPs ranged from 1.6 to 3.0, and increased significantly with the increase of Kow values for most marine biota species, indicating that Kow was the major factor controlling the bioaccumulation of SCCPs and that SCCPs with higher lipophilicity were more prone to being bioaccumulated from water. Opposite to that observed for log BAFs, biota-sediment accumulation factors of specific SCCPs (range: 0.01–30) decreased significantly with the increase of Kow values. The biomagnification factor of total SCCPs for oyster–mangrove crab was 2.40, implying the potential biomagnification of SCCPs for benthos in the PRE.

Ecological Success of the Nitrosopumilus and Nitrosospira Clusters in the Intertidal Zone.

The intertidal zone is an important buffer and a nitrogen sink between land and sea. Ammonia oxidation is the rate-limiting step of nitrification, conducted by ammonia-oxidizing archaea (AOA) and ammonia-oxidizing bacteria (AOB). However, it remains a debatable issue regarding dominant ammonia oxidizers in this region, and environmental factors driving their spatiotemporal niche differentiation have yet to be identified. In this study, intertidal and subtidal zones of Zhoushan Islands were selected for seasonal sampling. Ammonia-oxidizing activity, quantitative PCR, and 454 high-throughput sequencing were performed to study the nitrification potential, abundance, and community structure of ammonia-oxidizing archaea and bacteria. AOA and AOB amoA abundance (107-108amoA gene copies/g dry weight sediment) varied spatiotemporally independently of environmental factors. AOA surpassed AOB in most samples, driven by sediment temperature, moisture, and total nitrogen. The diversity of both AOA and AOB differed spatiotemporally. The Nitrosopumilus and Nitrosospira clusters accounted for an absolutely dominant percentage of AOA (> 99%) and AOB (> 99%) respectively, indicating a negligible contribution of other clusters to ammonia oxidation. However, there was no significant correlation between nitrification potential and the abundance of AOA or AOB. Overall, the present study showed that AOA dominated over AOB spatiotemporally in the intertidal zone of Zhoushan Islands due to fluctuations in environmental factors, and the Nitrosopumilus and Nitrosospira clusters ecologically succeeded in the intertidal zone of Zhoushan Islands.

Ladderane records over the last century in the East China sea: Proxies for anammox and eutrophication changes

Anaerobic ammonium oxidation (anammox), an important process for converting fixed nitrogen to N2, plays an important role in the present-day marine nitrogen cycle. However, little is known about anammox activities in the past, especially in regions that were strongly affected by human activities, evidenced by eutrophication and hypoxia, which promote anammox bacteria growth. In this study, ladderanes have been measured in a sediment core and suspended particulate matter (SPM) in the East China Sea (ECS), to reconstruct the anammox record and to evaluate its responses to eutrophication and hypoxia. The detection and distribution of different ladderane lipids in SPM provide additional evidence that ladderanes were mostly produced in the water column and could reflect anammox activities. Summed ladderane content from the core varied between 11 and 300 ng/g dry weight (dw) sediment, with C20-[5]-ladderane fatty acid methyl esters (FAME) as the predominant compound (5–150 ng/g dw), followed by C20-[3]-ladderane FAME (1–110 ng/g dw), C18-[3]-ladderane FAME (1–32 ng/g dw) and C18 -[5]-ladderane FAME (3–11 ng/g dw). The detection of ladderanes over the last century indicate the existence of anammox in the past. The rapidly increasing trend of ladderanes since the 1960s correlates with an increase in phytoplankton biomarkers (Σ(B + D + A), brassicasterol (B), dinosterol (D) and C37 alkenones (A)), indicating that eutrophication exacerbated anammox growth. The co-variation between our ladderane record and published records of low-oxygen tolerant foraminiferal microfossils and hypoxia events over the past 60 years suggested that sediment ladderanes are a useful indicator for past changes of oxygen depletion or hypoxia in the ECS.

Distribution of phthalate esters in air, water, sediments, and fish in the Asan Lake of Korea

Phthalate esters (PEs) are the most commonly used plasticizers and one of the endocrine disrupting chemicals (EDCs) which are extensively present in various environment. Therefore, it is important to examine the levels and distribution of phthalates in multimedia environment. This study investigated the seasonal and spatial variation of 14 PEs in air, water, sediments, and fish in the Asan Lake. Asan Lake is one of the largest artificial lakes in Korea, and is surrounded by industrial complex and farmlands. The PEs were found to be present throughout the study area. The mean concentration of total PEs (∑14 PEs) was 3.92–33.09 ng/m3 in air, not detected (n.d.)-2.29 μg/L in water, 3.6–8973 μg/kg dry weight (dw) in sediment, and n.d.-1081 μg/kg dw in fish, respectively. The most frequently detected phthalate in the samples was di(2-ethylhexyl) phthalate (DEHP), and followed by di-n-butyl phthalate (DBP). The concentrations of PEs in water and sediment samples tended to decrease moving downstream of Asan Lake. Bioaccumulation of PEs showed that benthic feeding fish such as crucian carp or skygager contained higher levels of DEHP. Partitioning of DEHP and DBP between water and sediment was calculated using paired sediment/water samples and fugacity fraction (ff). High ff value (ff = 0.89 ± 0.1) of DBP and low ff value of DEHP (ff = 0.24 ± 0.1) confirmed that DEHP is the most abundant PEs in the sediment, and DBP is the second most abundant PEs except DEHP in water. Our results can provide important information of the distribution and behavior of PEs in the lake environment.

Algae sediment dynamics are mediated by herbivorous fishes on a nearshore coral reef

Epilithic algae are a ubiquitous component of coral reefs. Components of the epilithic algal matrix (EAM) can have a significant influence on coral settlement and benthic feeding by fishes. We employed a herbivore exclusion experiment on a fringing reef in Viti Levu, Fiji, to investigate the functional role of herbivorous fishes in affecting the EAM between different habitat types and levels of community-based fishing restriction. We surveyed the herbivorous fish community and deployed experimental tiles on the reef flat and lagoonal slope and inside and outside of an area where fishing is restricted (tabu). Tiles were deployed for 3 months, half within cages to exclude herbivorous fishes. We then identified algal type and quantified epilithic algal turf height, sediment dry weight, and detritus within the EAM on each tile. EAM that developed under herbivory was remarkably similar, regardless of the differences in habitat or fishing restriction. In contrast, EAM within cages was characterised by longer turf, heavier sediment load, and high variance in turf length and sediment load. Habitat type played a strong role in determining EAM characteristics where herbivores were excluded. Caged EAM on the reef flat was characterised by algal turf and fleshy macroalgae, whereas EAM in cages on the lagoonal slope was overwhelmingly dominated by filamentous and mat-forming cyanobacteria. The results presented here demonstrate the importance of herbivorous fishes in maintaining a benthic environment favourable to coral settlement and survival. Our results suggest that herbivore biomass per se is not a reliable predictor of foraging activity. Moreover, these results show that the absence of herbivore foraging can have different consequences depending on the habitat type, even within the same reef.

Algal scavenging of mercury in preindustrial Arctic lakes

AbstractThe geochemical speciation of total mercury (THg) was examined in pre‐1800 Arctic lake sediments to improve understanding of the factors controlling “natural baseline” THg. Solid‐phase binding forms of THg were determined by sequential extraction of dated cores from three lakes in different ecozones (barren tundra, grassy tundra, and boreal forest). Sediment organic matter (OM) was mostly of algal origin. Mercury was highly concentrated in the sediment OM fraction (OM‐Hg), comprising 60–87% of THg, while OM (as total organic carbon) constituted only 0.6–13% of sediment dry weight (DW). OM‐Hg concentrations were equivalent to 159 ± 13 to 776 ± 215 ng Hg g−1 DW in algal OM and were enriched 2–39 times compared to sediment THg, indicating that even small changes in algal OM inputs could significantly alter THg. OM‐Hg explained 76–96% of the variation in THg concentrations over many centuries. Concentrations of S2 carbon (an algal productivity proxy) and OM‐Hg were significantly correlated in two lakes but not in the boreal forest lake possibly because of OM remineralization in its deep water column. Fluxes of S2 carbon, OM‐Hg, and THg were highly correlated in the barren tundra lake but could not be calculated for the other lakes. The results overall indicate that high algal Hg concentrations due to scavenging of available Hg controlled OM‐Hg flux to sediments, thus driving changes in THg concentrations and fluxes. These findings improve our understanding of the long‐term stability of baseline THg in northern lakes under a changing climate, including in the modern era.

Response of sediment bacterial community to triclosan in subtropical freshwater benthic microcosms

The response of sediment bacterial communities in subtropical freshwater benthic microcosms to sediment-associated triclosan (TCS; 28 d exposure) was analysed using Illumina high-throughput sequencing. This study highlights the interactive effects of TCS and the presence of benthic macroinvertebrates (Limnodrilus hoffmeisteri and Viviparidae bellamya) on sediment bacterial communities. Our results show that TCS alone significantly altered the taxonomic composition and decreased alpha diversity of sediment bacterial communities at concentrations ≥80 μg TCS/g dry weight (dw) sediment (sed). Regarding dominant phyla, TCS significantly reduced the relative abundance of Bacteroidetes and Firmicutes at these concentrations, whereas the relative abundance of Chloroflexi and Cyanobacteria increased. In the presence of benthic macroinvertebrates, the sediment bacterial community was affected by 8 μg TCS/g dw sed as well. However, the presence of benthic macroinvertebrates did not cause measurable changes to bacterial community in unspiked (i.e., control) sediment. These results indicate that TCS alone would not alter the sediment bacterial community at environmentally relevant concentrations (up till 8 μg/g dw sed), but may have an effect in combination with the presence of benthic macroinvertebrates. Therefore, we recommend to include benthic macroinvertebrates when assessing the response of sediment bacterial communities during exposure to environmental stress such as organic contaminants.

Insights into the sediment toxicity of personal care products to freshwater oligochaete worms using Fourier transform infrared spectroscopy

Personal care products (PCPs) are ubiquitous in the environment due to their wide use in daily life. However, there are insufficient sediment toxicity data of PCPs under ecologically relevant conditions. Here we used Fourier transform infrared spectroscopy (FTIR) to investigate the sediment toxicity of triclosan (TCS) and galaxolide (HHCB) to two freshwater benthic macroinvertebrates, Limnodrilus hoffmeisteri and Branchiura sowerbyi, in microcosms containing a diverse biological community. Exposure to 8 µg TCS/g and 100 µg HHCB/g dry weight (dw) sediment induced significant biochemical alterations in the L. hoffmeisteri tissue. 8 µg TCS/g primarily affected proteins and nucleic acid while 100 µg HHCB/g mainly affected proteins and lipids of L. hoffmeisteri. However, 0.8 µg TCS/g and 30 µg HHCB/g did not cause significant subcellular toxicity to L. hoffmeisteri. In contrast, exposure of B. sowerbyi to 30 µg HHCB/g led to significant biochemical changes, including proteins, polysaccharides and lipids. Therefore, B. sowerbyi was more sensitive to sediment-associated HHCB than L. hoffmeisteri. Such effects were significantly enhanced when the HHCB concentration increased to 100 µg/g dw where death of B. sowerbyi occurred. These results demonstrate the application of FTIR spectroscopy to sediment toxicity testing of chemicals to benthic invertebrates with biochemical alterations as endpoints that are more sensitive than standard toxic endpoints (e.g., survival and growth).

Biomarker responses and biotransformation capacity in Arctic and temperate benthic species exposed to polycyclic aromatic hydrocarbons

Monitoring parameters for the assessment of oil and gas related contaminants and their biological effects need validation before application in the Arctic. For such monitoring purposes, we evaluated the potential use of three biomarkers (acetylcholinesterase, acyl-CoA oxidase and glutathione S-transferase) for application to an Arctic bivalve (Astarte borealis) and determined the body residue of pyrene and two pyrene metabolites (1-hydroxypyrene and pyrene-1-glucuronide) in Arctic benthic species (bivalve: Macoma calcarea; polychaete: Nephtys ciliata) and temperate benthic species (bivalve: Limecola balthica; polychaete: Alitta virens) in order to establish the potential of polycyclic aromatic hydrocarbons (PAHs) metabolite profiles as biomarkers of exposure in such species. Experimental PAH exposure levels were probably too low (0.2–1.7 mg/kg dry weight in sediment) to induce or inhibit biomarker responses in A. borealis. Concentrations of pyrene and pyrene metabolites varied between species, although no consistent patterns could be established among taxonomic groups and locations. Metabolites made up to 79% of the total pyrene concentrations, indicating that basal metabolic activity is affecting pyrene kinetics even at low concentrations in all species. This indicates that Arctic and temperate species could show similar metabolism patterns of PAHs, although more insight into the effects of confounding factors is needed.