Biochemical indicators for the bioavailability of organic carbon in ground water

The bioavailability of total organic carbon (TOC) was examined in ground water from two hydrologically distinct aquifers using biochemical indicators widely employed in chemical oceanography. Concentrations of total hydrolyzable neutral sugars (THNS), total hydrolyzable amino acids (THAA), and carbon-normalized percentages of TOC present as THNS and THAA (referred to as "yields") were assessed as indicators of bioavailability. A shallow coastal plain aquifer in Kings Bay, Georgia, was characterized by relatively high concentrations (425 to 1492 μM; 5.1 to 17.9 mg/L) of TOC but relatively low THNS and THAA yields (∼0.2%–1.0%). These low yields are consistent with the highly biodegraded nature of TOC mobilized from relatively ancient (Pleistocene) sediments overlying the aquifer. In contrast, a shallow fractured rock aquifer in West Trenton, New Jersey, exhibited lower TOC concentrations (47 to 325 μM; 0.6 to 3.9 mg/L) but higher THNS and THAA yields (∼1% to 4%). These higher yields were consistent with the younger, and thus more bioavailable, TOC being mobilized from modern soils overlying the aquifer. Consistent with these apparent differences in TOC bioavailability, no significant correlation between TOC and dissolved inorganic carbon (DIC), a product of organic carbon mineralization, was observed at Kings Bay, whereas a strong correlation was observed at West Trenton. In contrast to TOC, THNS and THAA concentrations were observed to correlate with DIC at the Kings Bay site. These observations suggest that biochemical indicators such as THNS and THAA may provide information concerning the bioavailability of organic carbon present in ground water that is not available from TOC measurements alone.     

Sediment dynamics in the Castleton karst,Derbyshire, U.K.

Chemical and mineralogical data are presented for a suite of 59 sediment samples collected from the P8 and Speedwell cave systems (and mineralogical data are presented for a further six surface sediments) in the Castleton karst catchment, Derbyshire, England. Sediments are grouped according to age and depositional environment and these groups show distinctive mineralogical and chemical characteristics. Clay mineralogy is effective at distinguishing different sediment sources for ancient and modern sediments which are derived from pre-Devensian tills and Devensian solifluction deposits, respectively. Major element chemistry reflects these differences in clay mineral content, while trace elements demonstrate the importance of abrasion of ore minerals in conduits in the aquifer which follow mineral veins, even under natural, pre-mining conditions. Clay minerals are confirmed as the host for uranium in uranium-rich ancient sediments. Consideration of organic carbon and hydrogen concentrations shows that plant material is the dominant source of organic material in the modern sediments. Copyright © 1999 John Wiley & Sons, Ltd.     

Evidence for Enhanced Mineral Dissolution in Organic Acid-Rich Shallow Ground Water

Total concentrations of formate, acetate, and isobutyrate varied from less than 5 to greater than 9,000 μmol/l over distances of < 3 m in ground water from a shallow hydrocarbon contaminated aquifer. Laboratory incubations of aquifer material indicate that organic acid concentrations were dependent on the amount of hydrocarbon loading in the sediment and the relative rates of microbial organic acid production and consumption. In heavily contaminated sediments, production greatly exceeded consumption and organic acid concentrations increased. In lightly contaminated sediments rates were essentially equal and organic acid concentrations remained low. Concentrations of dissolved calcium, magnesium, and iron generally were one to two orders of magnitude higher in organic acid-rich ground water than in ground water having low organic acid concentrations. Carbonate and Fe(III)-oxyhydroxide minerals were the likely sources of these elements. Similarly, concentrations of dissolved silica, derived from quartz and k-feldspar, were higher in organic acid-rich ground water than in other waters. The positive relation (r = 0.60, p < .05, n = 16) between concentrations of silica and organic acids suggests that the microbially mediated buildup of organic acids in ground water enhanced quartz/k-feldspar dissolution in the aquifer, although it was not the only factor influencing their dissolution. A model that included organic acid microequivalents normalized by cation microequivalents significantly strengthened the correlation (r = 0.79, p < .001, n = 16) between dissolved silica and organic acid concentrations, indicating that competition between silica and cations for complexation sites on organic acids also influenced quartz/k-feldspar dissolution. Physical evidence for enhanced mineral dissolution in organic acid-rich waters included scanning electron microscopy images of highly corroded quartz and k-feldspar grains from portions of the aquifer containing organic acid-rich ground water. Microporosity generated in hydrocarbon contaminated sediments may adversely affect remediation efforts that depend on the efficient injection of electron acceptors into an aquifer or on the recovery of solutes from an aquifer.     

Long-Term Evaluation of Mulch Biowall Performance to Treat Chlorinated Solvents

Permeable reactive barriers (PRBs), such as mulch biowalls, have been installed at numerous groundwater cleanup sites, and laboratory and field studies have demonstrated biotic and abiotic processes that degrade chlorinated volatile organic compounds (CVOCs) in groundwater passing through these engineered remedies. However, the longevity of mulch biowalls remains a fundamental research question. Soil and groundwater sampling at seven mulch biowalls at Altus Air Force Base (AFB) approximately 10 years after installation demonstrated the ongoing degradation of CVOCs. Trichloroethene was not detected in five of seven groundwater samples collected from the biowall despite upgradient detections above federal drinking water standards. Microbial sampling established the presence of key dechlorinating bacteria and the abundance of genes encoding specific enzymes for degradation, high methane concentrations, low sulfate concentrations, and negative oxidation-reduction potential, all indicative of highly reducing conditions within the biowalls and favorable conditions for CVOC destruction via microbial reductive dechlorination. High cellulose content (>79%) of the mulch, elevated total organic carbon (TOC) content in groundwater, and elevated potentially bioavailable organic carbon (PBOC) measurements in soil samples further supports an ongoing, long-lived source of carbon. These results demonstrate the ongoing and long-term efficacy of the mulch biowalls at Altus AFB. In addition, concentrations of bacteria, TOC, PBOC, and other geochemical parameters suggest a modest impact of the biowalls downgradient. The continued presence of CVOCs downgradient may be attributable to back diffusion from low-permeability shale. However, the biowalls continue to provide benefits by removing CVOCs in groundwater, thus reducing further CVOC loading to the downgradient, low-permeability strata.     

Bacterial and organic matter distribution in the sediments of the Thracian Sea (NE Aegean Sea)

Recently, black carbon has been introduced as the form of carbon that may be separated from the biologically mediated carbon cycle thereby representing the non-bioavailable fraction of the estimated organic carbon. It has been speculated that the bioavailability of organic matter may be a limiting factor for the presence of active bacteria within the sediments. In order to address this question, marine sediments were collected from the Thracian Sea (Eastern Mediterranean), a complex system impacted by riverine inputs and Black Sea water masses. In addition to counts of total bacteria, we estimated the fraction of active bacteria by using a destaining step to the DAPI staining method. Black carbon was also estimated following the thermal oxidation method in order to determine the fraction of the refractory organic matter. The fraction of black carbon to total organic carbon varied from 16% to 53% indicating that black carbon constitutes a significant pool of sedimentary organic carbon in the Thracian sea. A fraction ranging from 18% to 97% was scored as nucleoid containing cells. We did not record any significant differences in the fraction of nucleoid-containing bacteria among sediment depths (P<0.05) indicating that there was no accumulation of dead bacterial cells with depth. The same was observed for the fraction of black carbon and bioavailable organic carbon with sediment depth (P<0.05) indicating that benthic consumers are not the key regulators of the organic matter pool in these sediments but have a minor effect. A possible reason for these observations and for the uncoupling between the active bacterial fraction and the bioavailability of organic matter could be (i) the presence of refractory components in the estimated bioavailable organic matter and (ii) the hydrological and geological complexity of the study area. The North Aegean marginal slopes are highly unstable experiencing frequent seismic events. These events are capable of inducing sediment transport from the upper slopes thus altering the entire sediment profile. On the other hand, the significant correlations that were recorded between nucleoid-containing cells and phytopigments (chlorophyll a, phaeopigments, chloroplastic pigment equivalents) at all sediment depths indicate that bacterial communities respond immediately to the deposited phytodetritus, using it as a primary source of carbon and energy. Our data suggests that the Thracian Sea sediments are by no means homogeneous and can best be described as a mosaic controlled by numerous local and regional environmental factors.     

鄱阳湖西侧周边农村水塘夏季表层沉积物氮、磷、有机质分布特征及评价

水塘作为农村重要的水生态系统,其环境状况与人们生产生活和健康密切相关。为了解鄱阳湖西侧周边农村水塘沉积物的有机质和营养盐赋存状况,于2018—2019年对鄱阳湖流域西侧附近4个县的23个水塘进行沉积物营养盐的分析,同时通过相关分析和差异性分析对其来源进行解析,并采用综合污染指数评价法和主成分分析法对水塘沉积物的污染程度进行评价。结果表明：水塘沉积物污染物含量较高,其有机质、有机碳（TOC）、总氮（TN）和总磷（TP）含量分别为5.81%±2.16%、2.46%±1.02%、（6.48±2.35） mg/g和（1.89±0.80） mg/g。3种形态的无机氮中铵态氮含量最高,其次为硝态氮和亚硝态氮。沉积物TP受到洗涤废水的影响较大,清淤和活化显著减轻了沉积物TN和TOC污染。综合污染指数评价结果表明重度污染和中度污染的水塘占比分别为95.65%和4.35%,其平均评价结果为重度污染,表明水塘沉积物污染严重。而主成分分析结果表明P18水塘污染最重,而P6水塘污染最轻。综合污染指数与主成分分析总得分的相关系数为0.92,表明两者的评价结果较为一致。本研究通过分析鄱阳湖西侧农村水塘的沉积物营养...     

Oxygen-enhanced biodegradation of phenoxy acids in ground water at contaminated sites

The effects of adding oxygen to anaerobic aquifer materials on biodegradation of phenoxy acid herbicides were studied by laboratory experiments with aquifer material from two contaminated sites (a former agricultural machinery service and an old landfill). At both sites, the primary pollutants were phenoxy acids and related chlorophenols. It was found that addition of oxygen enhanced degradation of the six original phenoxy acids and six original chlorophenols. Inverse modeling on 14C 4-chloro-2-methylphenoxypropanoic acid (MCPP) degradation curves revealed that increasing the oxygen concentrations from <0.3 mg/L up to 7 to 8 mg/L shortened the lag phases (from approximately 150 d to 5 to 25 d) and increased first-order degradation rate constants by 1 order of magnitude (from approximately 5 x 10(-2) d(-1) to up to 30 x 10(-2) d(-1)). Additionally, the degree of MCPP mineralization was increased (30% to 50% mineralized at low oxygen concentrations and 50% to 70% mineralized at high oxygen concentrations, based on 14CO2 recovery). These positive effects on degradation were observed even at relatively low oxygen concentrations (2 mg/L). Furthermore, effects related to the addition of oxygen on the general geochemistry were studied. An oxygen consumption of 2.2 to 2.6 mg O2/g dw was observed due to oxidation of solid organic matter and, to some extent (0.5% to 11% of the total oxygen consumption), water-soluble compounds such as Fe2+, dissolved Mn, nonvolatile organic carbon, and NH4+. Overall, the results suggest that stimulated biodegradation by addition of oxygen might be a feasible remediation technology at herbicide-contaminated sites, although oxygen consumption by the sediment could limit the applicability.     

The dynamics of sediment‐associated contaminants over a transition from drought to multiple flood events in a lowland UK catchment

Fine sediment in suspended form, recently deposited overbank and in temporary storage on or in channel beds, was collected in the Nene basin during a period of drought through to a period of four high flows. The sediment was analysed for arsenic, copper, lead, phosphorus and zinc concentrations with the aim of investigating their sources, movement, temporary storage and potential for environmental harm. Copper, lead and zinc probably originated from urban street dusts, phosphorus (originally in dissolved form) from sewage effluent and arsenic from natural soils developed over ironstone. There was little difference in the metal or arsenic concentrations in the sediment under different flow conditions; instead, proximity to pollutant sources appeared to control their concentrations. Phosphorus in tributary sub‐catchments probably adsorbed to sediment during periods of low flow but these sediments were flushed away during high flows and replaced by sediment with lower concentrations. However, concentrations of all pollutants in overbank sediments along the Nene's main channel were not reduced in successive flood events, suggesting no first flush effect. Only phosphorus accumulated on sediment at concentrations exceeding those of its catchment‐based sources (e.g. street dusts, channel banks and catchment soils). This scavenging of aqueous phosphate by sediment explained the difference in behaviour between phosphorus, arsenic and heavy metals. The surface area and organic matter content were shown to have a small effect on contaminant concentrations. Street dust contaminants only exceeded predicted effect levels in close proximity to urban areas, suggesting a small potential for harm to the aquatic environment. Arsenic concentrations exceeded predicted effect levels in most sediment samples. However, it has been shown to be largely non‐bioavailable in previously published research on the Nene, limiting its potential for significant environmental harm. Phosphorus concentrations in river sediments are high in comparison to the soils in the catchment and in comparison with sediment–P concentrations in other published lowland catchment studies, indicating a large potential for eutrophication should the Phosphorus be, or become, bioavailable. Copyright © 2015 John Wiley & Sons, Ltd.     

Heavy metal contamination in western Xiamen Bay sediments and its vicinity, China

Concentrations of selected heavy metals (Cu, Pb, Zn, Cd, Cr, Ni and Fe) in surface sediments from nine sites in western Xiamen Bay and its vicinity were studied in order to understand current metal contamination due to urbanization and economic development in Xiamen, China. The sediment samples were collected in December 2004 and July 2005 respectively in order to examine temporal variations. In this study, we found that heavy metal concentrations in surface sediments sampled in the western Xiamen Bay and adjacent Maluan Bay and Yuandang Lagoon varied from 19 to 97mg kg(-1) for Cu, 45 to 60mg kg(-1) for Pb, 65 to 223mg kg(-1) for Zn, 0.11 to 1.01mg kg(-1) for Cd, 37 to 134mg kg(-1) for Cr, 25 to 65mg kg(-1) for Ni and 3.08 to 4.81% for Fe. Although all metal concentrations in sediments meets Chinese National Standard Criteria for Marine Sediment Quality, both metal enrichment factors (EF) and geoaccumulation index (I(geo)) show that Pb contamination exists in the entire study area and contamination of other metals are also present in some locations depending on the sources, of which sewage outlets and commercial ports are the main sources of contaminants to the area. This study shows that using the sediment quality standard criteria only to assess sediments cannot properly reflect sediment contamination. A multiple approaches should be applied for the sediment quality assessment.     

Content and distribution of trace metals in surface sediments from the northern Bering Sea, Chukchi Sea and adjacent Arctic areas

Concentrations of trace metals (Zn, Cr, Cu, V, Cd and Pb), total organic carbon (TOC), black carbon (BC) and their granulometry were examined in 25 surface sediment samples from the northern Bering Sea, Chukchi Sea and adjacent areas. Trace metal concentrations in the sediments varied from 21.06-168.21 mg kg(-1) for Zn, 8.91-46.94 mg kg(-1) for Cr, 2.69-49.39 mg kg(-1) for Cu, 32.46-185.54 mg kg(-1) for V, 0.09-0.92 mg kg(-1) for Cd, and 0.95-15.25 mg kg(-1) for Pb. The geoaccumulation index (Igeo) indicated that trace metal contamination (Zn and Cd) existed in some stations of the study area. The distribution of grain size plays an important role in influencing the distribution of trace metals (Zn, Cr, Cu, V, and Pb) in sediments from the Chukchi Sea and adjacent areas.     

坦噶尼喀湖东北部入湖河流表层沉积物中磷的形态和分布特征

磷是坦噶尼喀湖生态系统中必不可少的营养元素,直接决定湖体初级生产力的高低,进而影响到周边居民对于动物蛋白的获取来源.为了解坦噶尼喀湖磷的外源输入,选择湖泊东北部的入湖河流,对表层沉积物(16个样点)中总磷(TP)和各形态磷含量及其分布特征进行分析,并探讨磷的形态分布特征与土地利用方式之间的相关关系.结果表明,入湖河流沉积物TP含量为73.05~239.94 mg/kg,平均含量为152.64±55.37 mg/kg,其中最高值出现在马拉加拉西河口.采用Psenner法对磷进行连续浸提并比较不同形态磷含量,由高及低依次为铁铝结合态磷(Fe/Al-P)钙结合态磷(CaP)有机磷(Org-P)残渣态磷(Res-P)弱吸附态磷(Labile-P).土地利用类型对TP及各形态磷含量影响较大,其中TP含量表现为河口湿地城镇附近林草地区,表明地表径流和人类活动会对TP含量产生影响,而对于不同形态磷含量,Laible-P、Fe/Al-P、Org-P含量均表现为河口湿地林草地城镇附近,Ca-P、Res-P含量均表现为城镇附近河口湿地林草地.分析沉积物理化性质与各磷形态之间的相关性,发现沉积物总氮(TN)、有机质和总有机碳与Fe/Al-P、LabileP和TP相关性较好,与Org-P、Ca-P和Res-P相关性较差,表明TN和有机质的输入,会伴随沉积物中磷含量的升高,其增量的赋存形态主要为氧化还原敏感态磷和Labile-P.沉积物粒径组成与各磷形态含量存在相关性,细粒径沉积物与各形态磷含量呈显著正相关,粗粒径沉积物与各形态磷呈显著负相关,表明细小颗粒更易吸附磷.     

Estimating suspended sediment concentrations from turbidity measurements and the calibration problem

In situ turbidity meters are being increasingly used to generate continuous records of suspended sediment concentration in rivers. However, the usefulness of the information obtained depends heavily on the existence of a close relationship between fluctuations in suspended sediment concentration and turbidity and the calibration procedure that relates suspended sediment concentration to the turbidity meter's signal. This study assesses the relationship between suspended sediment concentration and turbidity for a small (1·19 km²) rural catchment in southern Brazil and evaluates two calibration methods by comparing the estimates of suspended sediment concentration obtained from the calibrated turbidity readings with direct measurements obtained using a USDH 48 suspended sediment sampler. With the first calibration method, the calibration relationship is derived by relating the turbidity readings to simultaneous measurements of concentration obtained from suspended sediment samples collected from the vicinity of the turbidity probe during flood events. With the second method, the calibration is based on the readings obtained from the turbidity meter when the probe immersed in samples of known concentration prepared using soils collected from the catchment. Overall, there was a close link between fluctuations in suspended sediment concentration and turbidity in the stream at the outlet of the catchment, and the estimates of sediment concentration obtained using the first calibration method corresponded closely with the conventionally measured sediment concentrations. However, use of the second calibration method introduced appreciable errors. When the estimated sediment concentrations were compared with the measured values, the mean errors were ± 122 mg l^?1 and + 601 mg l^?1 for the first and second calibration procedures respectively. Copyright © 2007 John Wiley & Sons, Ltd.     

Present state and historical changes of trace metal pollution in Kaoping coastal sediments, southwestern Taiwan

Surface and gravity-cored sediments were collected from the Kaoping coastal area off southwestern Taiwan to determine particle size, organic carbon, trace metal concentration and enrichment factor (EF), 210Pb dating, and 206Pb/207Pb ratio for determining present and historical metal pollution. Surface distributions of trace metals ranged from 0.02 to 0.13 mg/kg for Cd (EF: 0.16-1.65), from 35 to 189 mg/kg for Cr (EF: 0.85-2.92), from 25 to 64 mg/kg for Ni (EF: 0.53-2.38), from 10 to 32 mg/kg for Pb (EF: 1.20-4.94), and from 29 to 129 mg/kg for Zn (EF: 1.18-3.50). Trace metal concentrations correlate closely with distributions of mud (<63 microm) and organic carbon which accumulate largely around river mouths and within the Kaoping Canyon. With the exception of Cd, Cr and Ni in certain areas with rather coarse sediments, metals were generally elevated above the baseline levels over the studied area. Metals were also relatively enriched in areas with high contents of mud and organic carbon. Sedimentation rates derived from the excess 210Pb data in core sediments sampled from the canyon illustrate metal pollution beginning around 1970 that is corresponding to the booming time of economic growth in Taiwan. Meanwhile, the status of Pb pollution in core sediments is verified by an inversed correlation between 206Pb/207Pb ratios and Pb concentrations. Anthropogenic Pb and other metals in the studied area were apparently derived primarily from the Kaoping River and accumulated around the river mouth and within the Kaoping Canyon. The Kaoping Canyon appears to act as a major sink for river borne trace metals.     

太湖沉积物理化性质及营养盐的时空变化

在不同季节,采集太湖梅梁湾和贡湖湾沉积物柱状样,研究沉积物Eh、pH、总氮、总磷以及有机质四季垂向剖面分布变化特征.研究结果表明,在表层下(0-3 cm),Eh随沉积物深度的增加迅速下降,很快进入还原状态.沉积物剖面上pH变化幅度不大,在6.4-7.8之间,冬季沉积物pH均有所降低.太湖沉积物中含有丰富的营养盐,总氮和总磷最高浓度分别为2.68和0.864 mg/g,其剖面分布特征表明,沉积物表层总氮和总磷含量远高于底层,其含量随深度增加而降低,但四季变化趋势不明显.沉积物中有机质含量在10 cm以上变化幅度较大,随着沉积物深度的增加,有机质含量明显减少,季节变化幅度不大.比较不同采样点发现,位于梅梁湾生态系统试验区内的S1位点沉积物氮磷内源负荷最大.     

洞庭湖平原中小型湖群沉积物中砷污染特征与评价

本文研究了洞庭湖平原10个中小型湖泊沉积物砷的空间分布特征,并采用地累积指数法对其污染进行了评价.结果表明:各湖表层沉积物中砷浓度在10.1 -33.7 mg/kg之间变化,平均值为15.8 mg/kg,砷含量水平较低;在空间上表层沉积物中砷含量次序为岳阳南湖＞芭蕉湖＞黄盖湖＞安乐湖＞毛里湖＞柳叶湖＞东湖＞珊珀湖＞大通...     

The burial efficiency of organic carbon in the sediments of Lake Kinneret

Even though lake sediments constitute a significant long-term carbon sink, studies on the regulation of carbon burial in lakes sediments have, to date, been surprisingly few. We investigated to what degree the organic carbon (OC) being deposited onto the bottom of Lake Kinneret (Israel) is buried in the sediment at four different sites with varying degrees of oxygenation and varying supply of allochthonous particles from the River Jordan. For estimation of the OC burial efficiency (OC BE), i.e., the ratio between buried and deposited OC, we calculated OC burial from dated sediment cores, and calculated OC deposition using three different approaches. Calculation of OC deposition from sediment trap-derived mass deposition rates multiplied with the OC content of surface sediment yielded OC BE values that were at odds with published values for sediments dominated by autochthonous OC sources. Calculation via sediment trap data on organic matter flux collected within the Lake Kinneret monitoring program, as well as calculation of OC deposition as the sum of OC burial plus OC mineralization, returned fairly congruent estimates of OC BE (range 10–41%), but only if the sediment trap data were corrected for the proportion of resuspended particles in the traps. Differences in OC BE between sites were small, indicating that OC source (common to all sites) was a more important regulator of OC BE in Lake Kinneret than oxygen exposure or mineral particles characteristics.     

The effects of sewage organic matter on biogeochemical processes within mid-shelf sediments offshore Sydney, Australia

A laboratory incubation experiment was conducted using replicate cores collected from a muddy-sand sediment facies offshore Sydney, Australia to determine what components and processes would be affected by the addition of sewage organic matter. Sewage effluent has a solid phase composition of 40% carbon (35% organic carbon), 5% nitrogen, 1% phosphorus and 5% silicate. The molecular C:N:P ratio is 92:10:1, compared to the Redfield ratio of 106:16:1 in marine phytoplankton. Sediment cores were incubated at in situ temperature in a darkened room for periods up to 95 days. Sewage organic matter was added to the cores at three different loads equivalent to 0 (T0), 65 (T1) and 130 (T2) g m⁻² of sediment. Following the addition of sewage organic matter, fluxes of oxygen (into the sediments), ammonia and phosphate (from the sediments) increased, reflecting an enhanced organic carbon supply to the sediments. Oxygen penetrated to a depth of 6 mm in the ambient cores, but the sediment oxygen content was severely depleted following the addition of the sewage-derived organic matter. Sediment porewater data, together with nutrient flux data indicate that oxygen reduction, nitrate reduction and sulphate reduction occurs within these sediments. Following the addition of sewage organic matter, increases in total nitrogen, total phosphate and total organic carbon were measured to depths of 5 cm in the sediments, suggesting that bioturbation influences nutrient and organic carbon distributions. Additionally, irrigation of the surficial sediments may play an important role in the metabolism of organic matter. These results indicate that oxygen penetration, oxygen fluxes, nitrate concentrations within porewaters, ammonia flux rates, and solid phase concentrations of total organic carbon and nutrients may be useful indicators of sediments affected by high rates of organic matter deposition onto Sydney's offshore sediments. The EPA has recently predicted maximum deposition rates of sewage particulate matter to be approximately 1 g m⁻² day⁻¹. Because of the similarities in CNP ratios of sewage organic matter and marine organic matter, the effects of sewage organic matter and marine organic matter inputs to coastal sediments may not be easily distinguishable.     

Carbon speciation and composition of natural microbial communities in polluted and pristine sediments of the Eastern Mediterranean Sea

Sediment samples collected from polluted (Augusta Bay) and pristine regions of the Eastern Mediterranean Sea (South Ionian Sea, Thracian Sea) were analyzed for black carbon, aliphatic hydrocarbons and phospholipid ester-linked fatty acids (PLFA). The aim of the study was to investigate the anthropogenic and biogenic inputs into the Eastern Mediterranean Sea and to evaluate the effects of refractory organic matter (e.g. black carbon) and the level of hydrocarbon contamination on benthic microbial community composition. Black carbon, generally considered to be chemically and biologically inert, comprised a significant but highly variable fraction of the sedimentary carbon pool in the analyzed sediments with a ratio to total organic carbon ranging from 0.02 to 0.66. Principal component analysis of the chemical characteristics of the sediments (organic carbon content, black carbon, bioavailable organic carbon, chlorophyll a, phaeopigments, aliphatic hydrocarbons) revealed clustering of samples along a gradient from the most productive and contaminated region of Augusta Bay to the carbon-poor and pristine sediments of the Thracian Sea. PLFA analysis revealed that gram-negative bacteria and microeukaryotes were most abundant in Augusta Bay and in the most impacted station of the Thracian Sea. The high levels of branched and odd-chain fatty acids recorded for these stations is probably linked to the elevated amounts of hydrocarbons at these stations; e.g. microbial communities may have developed the ability to degrade either naturally occurring aliphatic hydrocarbons or hydrocarbons derived from oil contamination.     

Correlation assessment and monitoring of the potential pollutants in the surface sediments of Pyeongchang River, Korea

The study provides a baseline for the assessment of the organic and inorganic pollution specially, heavy metal contamination in the surface sediments of Pyeongchang River,South Korea.The assessment of the study areas was done with respect to metal pollution load,ecological risk and geoaccumulated risk.Based upon the used indices,a priority index(P_index) was used to rank the utmost contaminated sites.Though the concentrations of mercury in all sediments were below the guideline, the significant enriched contamination was observed by all applied indices.As expected,the values of pollution load index（PLI）,ecological risk index（RI） and geoaccumulation risk index(I_geo) demonstrated lower heavy metal contamination in upstream areas compared to the downstream. Admittedly,sediments were unpolluted to slightly-polluted according to PLI while high to extremely high ecological risks were observed in several sediment samples.Furthermore,all the samples were uncontaminated as per I_geo.After simplification of I_geo,the P_index,showed the utmost contaminated sediments with a value of 2.537.Notably,protective measures should be taken to the highly contaminated areas which are prioritized by P_index Admittedly,the maximum concentrations of total organic carbon,total nitrogen,inorganic nitrogen,total phosphorous,inorganic phosphorous,calcium, magnesium,sodium and potassium were significantly observed as 7.8×10⁴,3,185,36,1,032,3.7, 1,5163,2,881,669 and 4,076mg/kg accordingly.     

Investigating the distribution and sources of organic matter in surface sediment of Coombabah Lake (Australia) using elemental,isotopic and fatty acid biomarkers

Extensive physical and biological measurements were made of the surface sediments within the shallow, semi-urbanised Coombabah Lake in southern Moreton Bay, Australia. Sediment bulk parameters (C/N ratios, δ¹³C and δ¹⁵N) and fatty acid biomarkers were used to determine distributions and sources of organic matter in the intertidal sediments. The determination of organic matter sources within coastal and estuarine settings is important in understanding the roles of organic matter as energy and nutrient sources. Spatial variability of biomarker values within the sediments were interpreted by thematic maps employing the Krigging algorithm. Grain size analysis indicated the lake was dominated by mud (<63 μm) in the southern (landward) and sand (>63 μm) in the northern (seaward) lake regions, respectively. Surface sediment organic C and N values ranged from 0.12% to 1.76% and 0.01% to 0.12% dry weight, respectively, and C/N ratios averaged 16.3±3.19%. Sedimentary δ¹³C values ranged from −26.1‰ to −20.9‰, with an average value of −23.9±1.0‰. Sedimentary δ¹⁵N values ranged from +1.7‰ to +4.8‰, with an average value of +2.8±0.8‰. Bulk sediment parameters suggested that sedimentary organic matter is provided predominantly by allochthonous sources in the form of fringing mangroves. Thirty-nine individual fatty acids were identified using gas chromatography–mass spectrometry. The mean contributions of long chain fatty acids (LCFAs), polyunsaturated fatty acids (PUFAs), saturated fatty acids (SAFAs) and bacterial fatty acids (BAFAs) were, respectively, 13.9±11.4%, 7.6±4.1%, 53.6±8.6% and 18.2±4.6% of the identified fatty acid methyl esters (FAMEs), with BAFAs occurring in all sampled sediments. Fatty acid compositions varied throughout lake sediments, which indicated spatial differences in autochthonous and allochthonous organic matter sources, including terrestrial and planktonic (i.e. zooplankton, diatoms and other algal species) sources. The contribution of organic matter from shoreline mangroves was confirmed by the presence of LCFAs and 18:2ω6 and 18:3ω3, which are markers for mangroves in this ecosystem. BAFAs were identified in increased proportions in sediments adjacent to urban developments and dominated by mud. Grain size was identified as a dominant factor in the fatty acid compositions and contributing values to FAME pool. Spatial patterns of C/N ratios, δ¹³C and δ¹⁵N values, and fatty acid biomarker contributions illustrated that there is a greater contribution of autochthonous and labile organic matter to the sedimentary organic matter pool in the northern (marine entrance) sediments compared to the more allochthonous sourced organic matter of the southern region of the lake. This study details the distribution and sources of organic matter within Coombabah Lake and illustrates the usefulness of a multiple biomarker approach in discriminating organic matter sources within estuarine environments.