Determination of dissolved organic matter in streamwater using visible spectrophotometry

Absorbance at 360 nm was measured on 44 filtered streamwater samples of different dissolved organic matter (DOM) contents. A regression equation of DOM on absorbance predicted DOM with a standard error of estimate of 1.26 mgl^?1, Use of a published equation relating dissolved organic carbon (DOC) to absorbance gave DOC values for the samples which were consistent with measured DOM. The method offers considerable potential for rapid quantification of dissolved organic matter concentrations in streamwater.     

Distribution,characteristics and potential impacts of chromophoric dissolved organic matter (CDOM) in Hudson Strait and Hudson Bay,Canada

The characteristics of chromophoric dissolved organic matter (CDOM) were studied in Hudson Bay and Hudson Strait in the Canadian Arctic. Hudson Bay receives a disproportionately large influx of river runoff. With high dissolved organic matter (DOM) concentrations in Arctic rivers the influence of CDOM on coastal and ocean systems can be significant, yet the distribution, characteristics and potential consequences of CDOM in these waters remain unknown. We collected 470 discrete water samples in offshore, coastal, estuarine and river waters in the region during September and October 2005. Mixing of CDOM appeared conservative with salinity, although regional differences exist due to variable DOM composition in the rivers discharging to the Bay and the presence of sea-ice melt, which has low CDOM concentrations and low salinity. There were higher concentrations of CDOM in Hudson Bay, especially in coastal waters with salinities <28$<28$, due to river runoff. Using CDOM composition of water masses as a tracer for the freshwater components revealed that river runoff is largely constrained to nearshore waters in Hudson Bay, while sea-ice melt is distributed more evenly in the Bay. Strong inshore–offshore gradients in the bio-optical properties of the surface waters in the Hudson Bay cause large variation in penetration of ultraviolet radiation and the photic depth within the bay, potentially controlling the vertical distribution of biomass and occurrence of deep chlorophyll maxima which are prevalent only in the more transparent offshore waters of the bay. The CDOM distribution and associated photoprocesses may influence the thermodynamics and stratification of the coastal waters, through trapping of radiant heating within the top few meters of the water column. Photoproduction of biologically labile substrates from CDOM could potentially stimulate the growth of biomass in Hudson Bay coastal waters. Further studies are needed to investigate the importance of terrestrial DOM in the Hudson Bay region, and the impact of hydroelectric development and climate change on these processes.     

Organic geochemical studies of sinking particulate material in China sea area(I)

Sinking particulate material collected from Nansha Yongshu reef lagoon and the continental shelf of the East China Sea by sediment traps has been analyzed and studied for the first time using organic geochemical method. The results show that about half of the sinking particulate organic matter in the two study areas are consumed before reaching the depth of 5 m to the sea floor and the degree of this consumption in Yongshu reef lagoon is larger than that in the continental shelf of the East China Sea. The distributions of hydrocarbons and fatty acids indicate that the minor difference of biological sources of sinking particulate organic matter exists between Yongshu reef lagoon and the continental shelf of the East China Sea, but they mainly come from marine plankton. Stronger biological and biochemical transformations of sinking particulate organic matter are also observed and the intensity of this transformation in Yongshu reef lagoon is greater than that in the continental shelf of the East China Sea. It is found that the occurrence of C₂₅ highly branched isoprenoid (HBI) diene may be related to the composition of diatom species.     

The freshwater dissolved organic matter fluorescence–total organic carbon relationship

The fluorescent properties of dissolved organic matter (DOM) enable comparisons of humic‐like (H‐L) and fulvic‐like (F‐L) fluorescence intensities with dissolved organic carbon (DOC) in aquatic systems. The fluorescence‐DOC relationship differed in gradient, i.e. the fluorescence per gram of carbon, and in the strength of the correlation coefficient. We compare the fluorescence intensity of the F‐L and H‐L fractions and DOC of freshwater DOM in north Shropshire, England, featuring a river, wetland, spring, pond and sewage DOM sources. Correlations between fluorescence and DOC varied between sample sites. Wetland water samples for the F‐L peak gave the best correlation, r = 0·756; the lowest correlation was from final treated sewage effluent, r = 0·167. The relationship between fluorescence and DOC of commercially available International Humic Substances Society standards were also examined and they generally showed a lower fluorescence per gram of carbon for the F‐L peak than the natural samples, whereas peat wetland DOM gave a greater fluorescence per gram of carbon than river DOM. Here, we propose the strength of the fluorescence–DOC correlation to be a useful tool when discriminating sources of DOM in fresh water. Copyright © 2007 John Wiley & Sons, Ltd.     

Spectroscopic investigation of humic substances in a tropical lake during a complete hydrological cycle

Fluorescence and UV‐VIS techniques were employed for the investigation of natural organic matter (NOM) of a tropical lake. The relationships of absorbance/dissolved organic carbon (A/DOC), fluorescence intensity/dissolved organic carbon (FI/DOC), fluorescence ratio (FR), and peak wavelength with the highest intensity (PW) were used to distinguish the pedogenic or aquagenic origin of NOM. The values of FR, PW and A₂₈₅/DOC of high waters (HW) or flooded period samples and of low waters (LW) period samples of the dry season, except for September 2002, confirm the predominance of pedogenic material. The spectra of water were similar to the standard fulvic acid (FA), and the spectra of FA from the lake were similar to the nearby soils, indicative of pedogenic predominance. The results confirm that the dissolved NOM of Patos Lagoon – MS (Brazil), in all sampling periods, predominantly consisted of humic substances (FA) of pedogenic origin.     

Spectrophotometric discrimination of river dissolved organic matter

There is a need to be able to differentiate the dissolved organic matter (DOM) fraction in river waters. Research in the 1970s and 1980s has attempted to utilize both absorbance and fluorescence to distinguish between DOM fractions in river waters, but both were limited by the available technology. Total organic carbon content has, therefore, been widely used as a standard method of measuring DOM concentration, although it has little power to differentiate DOM fractions. Recent advances in fluorescence spectrophotometry enable rapid and optically precise analysis of DOM. Here, we show how a combination of both fluorescence and absorbance can be used to discriminate statistically between spatial variations of DOM in tributaries in a small catchment of the Ouseburn, NE England. The results of the discriminant analysis suggest that about 70% of the samples can be correctly classified to its tributary. Discriminant function 1 explains 60·8% of the variance in the data and the fulvic‐like fluorescence intensity has the largest absolute correlation within this function; discriminant function 2 explains a further 21·5% of the variance and the fulvic‐like fluorescence emission wavelength has the largest absolute correlation within this function. The discriminant analysis does not correctly classify all tributaries every time, and successfully discriminates between the different tributaries 70% of the time. Occasions when the tributary waters are less well discriminated are due to either episodic pollution events (at two sites) or due to tributaries that have strong seasonal trends in spectrophotometric parameters, which allows the sites to be misclassified. Results suggest that spectrophotometric techniques have considerable potential in the discrimination of DOM in rivers. Copyright © 2002 John Wiley & Sons, Ltd.     

Genesis and organic geochemical characteristics of the carbonaceous rock stratabound gold deposits, South China

The organic matter of three different chronological major carbonaceous rock gold-bearing formations of South China (Middle Proterozoic Shangqiaoshan group of northeastern Jiangxi, Lower Cambrian Shuikou group of northern Guangxi and Devonian Shetianqiao group of eastern Hunan) and related carbonaceous stratabound gold deposits such as Jinshan, Longshui and Shixia deposits, respectively, has been characterized by organic geochemical techniques. These organic geochemical results show that the average total organic carbon (TOC) content of the three chronological carbonaceous rock gold-bearing formations of South China ranges from 0.15% to 1.56%. The thermal maturity of the organic matter of host rocks in the three gold-bearing formations is high. The micro-component of the organic matter of the host rocks consists primarily of solid bitumen and graphite. The organic carbon and gold of the host rocks appear to syndepositin situ during the formation of the gold-bearing formations. The organic carbon played a certain role in controlling the geochemical environment of the gold-bearing formations. The metallogenetic mechanism of the carbonaceous rock stratabound gold deposits of South China is closely associated in genesis with the sedimentation, diagenesis and thermal evolution history of the organic matter of host rocks in the gold-bearing formations.     

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

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

不同时间尺度青海湖沉积物总有机碳对气候变化的敏感性

湖泊沉积物总有机碳（TOC）含量通常作为表征流域和湖泊生产力的指标,在亚洲季风区也常常被当作夏季风的代用指标,被广泛应用于气候与环境变化研究.本文梳理了过去千年、全新世以及冰期-间冰期时间尺度上青海湖沉积物TOC的变化特征,并探讨了其指示气候变化的敏感性与有效性.结果表明,过去千年青海湖沉积物TOC含量与区域暖季温度和降水表现出较为一致的周期性波动.通过对比全新世区域夏季温度、基于孢粉的降水定量重建结果,以及湖泊水位、风沙活动反映的湿度状况等,发现不能简单地将青海湖沉积物TOC含量或沉积通量作为夏季风强度或者季风降水强度的代用指标.青海湖沉积物TOC含量在冰期和间冰期表现出巨大的差异,指示了冰期-间冰期时间尺度上较大的温度与降水变幅.因此,不同地域条件及不同时间尺度下,湖泊沉积物TOC对气候变化的敏感性不同,将湖泊沉积物TOC含量作为亚洲夏季风的代用指标需要特别谨慎,特别是在高寒气候区.     

Dissolved organic carbon export from a cutover and restored peatland

High demand for horticultural peat has increased peatland drainage and peat extraction in Canada. The hydrology and carbon cycling of these cutover peatlands is greatly altered, necessitating active restoration efforts to permit the regeneration of Sphagnum mosses and the re‐establishment of natural peatland function. The effect of peatland extraction and restoration on the export of dissolved organic carbon (DOC) was examined for three successive seasons (May to October, 1999 to 2001) at two different sites (cutover and restored) in eastern Québec. A shift towards higher DOC concentrations was observed following peatland extraction (maximum: 182·6 mg L^?1) and concentrations remained high post‐restoration (maximum: 191·0 mg L^?1). The cutover site exported more DOC than the restored site in all three study seasons. The highest exports occurred during the wettest year (1999), with cutover and restored site export of 10·3 and 4·8 g m^?2, respectively. In 2000, 8·5 g C m^?2 was released from the cutover site, while the restored site released less than half that amount (3·4 g C m^?2). In 2001, the restored site released about the same amount of DOC as in the previous year (3·5 g C m^?2), while the cutover site load dropped to 6·2 g C m^?2. Both sites were net exporters of DOC in all years. Copyright © 2007 John Wiley & Sons, Ltd.     

Post-fire soil erosion mitigation at the scale of swales using forest logging residues at a reduced application rate

Mulching with forest residues has proved to be highly effective in reducing post-fire soil losses at the plot scale. However, its effectiveness has not been quantified at the application rates that are typically used in operational post-fire land management (2–3 Mg ha^-1 using straw), as well as at scales larger than 100 m². The present study compared post-fire erosion rates for six convergent hillslopes or swales of 500 to 800 m², three of which were left untreated while the other three were mulched immediately after the fire with shredded eucalypt bark at a rate of 2.4 Mg ha^-1. Erosion rates were monitored at irregular intervals during the first three post-fire years, whilst ground cover was assessed yearly. Selected topsoil properties (0–2 cm) such as organic matter content and aggregate stability were determined at a single occasion – two years after the wildfire, for three micro-environments separately: bare soil, and under mulch/litter and vegetation. Soil losses on the untreated swales decreased with post-fire year from 2.2 to 0.4 and 0.11 Mg ha^-1 yr^-1 (respectively for the first, second and third post-fire years), while the mulched swales produced 84%, 77% and 38% less soil losses than the untreated swales. Soil losses also depended on slope aspect, with the north-facing swales producing less erosion than the west-facing ones. This could be linked to their significant differences in bare soil, vegetation and stone cover, or a combination thereof. The type of micro-environment also played a significant role in topsoil properties (stone content, bulk density, resistance to penetration/shear stress, porosity and organic matter content). The present results add to the increasing evidence that forest residues should be duly considered for operational post-fire land management. Forest residues were highly effective in reducing erosion from swales at application rates as low as the typical 2 Mg ha^-1 of post-fire straw mulch. © 2019 John Wiley & Sons, Ltd. © 2019 John Wiley & Sons, Ltd.     

Reduced removal of bacteriophage MS2 in during basin infiltration managed aquifer recharge as basin sand is exposed to infiltration water

Basin infiltration managed aquifer recharge (MAR) is a commonly used method for storing and treating surface water to be used as drinking water. This study examined how the removal of bacteriophage MS2 was affected by the relative age of the sand used for basin infiltration MAR at 4 °C using batch experiments (static and agitated) and column experiments. The sand and the water used in all experiments were characteristic of that used at a basin infiltration MAR scheme in Uppsala, Sweden. Experimental data was fit with numerical models describing the fate and transport of virus in soil—water systems. The “used” sand that had been subjected to intermittent infiltration over a period of 8 years had 15 times the amount of organic carbon than the “new” sand, which had yet to be used for infiltration. Results showed that attachment of MS2 to the new sand in batch experiments was relatively irreversible. Attachment to the used sand was reversible. Inactivation of MS2 was slowed when it was attached to the used sand. Results for the column experiments showed that the removal rate of MS2 was significantly lower in columns of used sand than in columns of new sand. Simulations indicated that MS2 would be entirely removed in the infiltration basins with new sand. Less than 3 log removals was estimated for basins with used sand. Reduced removal of MS2 by the used sand was deemed to be most likely due to organic coatings on the used sand. Results of this study give deeper insight into the mechanisms responsible for removing virus in infiltration basins and how those mechanisms will change as the sand in the basin is exposed to infiltration water.     

江苏省西部湖泊溶解性有机物光谱学特征和来源解析

利用光谱学手段研究江苏省西部湖泊表层水体中溶解性有机物(DOM)组成与结构,并对其来源进行分析.单位浓度可溶性有机碳在254和280 nm波长下的吸光度值(SUVA)测定结果表明,各湖泊芳香性程度及分子量大小依次为邵伯湖>天岗湖>白马湖>石臼湖>洪泽湖>固城湖>骆马湖>高邮湖>宝应湖.特定波长下吸光度的比值(E2/E3、E3/E4)显示邵伯湖和白马湖中的DOM结构复杂、分子量大、苯环多,以腐殖酸为主要成分;其它湖泊的DOM腐殖化程度较低,以富里酸为主.指数函数曲线斜率(S275～295nm)拟合结果也同样表明邵伯湖DOM分子量最大,而宝应湖最低.各湖泊荧光指数和生物指数分别处于1.13～1.30和0.47～0.67范围内,体现出DOM强烈的陆源性.四个主要荧光峰的相对荧光强度之间均存在良好的相关性,表明这些湖泊的类腐殖酸及类蛋白物质可能有着相同的来源.结合这些湖泊的特征及流域经济发展水平,可以初步推断经入湖河流携带的由农业及其下游产业产生的有机质是江苏西部湖泊中DOM的主要来源.     

Erosion,deposition, and the persistence of soil organic matter: mechanistic considerations and problems with terminology

The effect of erosional detachment, transport, and deposition of topsoil on the stock of soil organic matter (SOM) and its association with soil minerals has been a focus of a growing number of studies. A particularly lively debate is currently centered on the questions of whether terrestrial sedimentation of previously eroded SOM may constitute a relevant sink for atmospheric carbon dioxide (CO₂), and how ‘stable’ such carbon (C) might be on multidecadal timescales. In this commentary, we illustrate how redistribution of eroded SOM within a landscape can create situations that are not adequately described by the jargon commonly used to characterize C turnover dynamics. We argue that more quantitative and scientifically rigorous categories are needed to describe soil C turnover and to promote the development of innovative, numerical models of C dynamics in landscapes characterized by significant mass movement. Copyright © 2013 John Wiley & Sons, Ltd.     

Retention of chloride in soil and cycling of organic matter‐bound chlorine

Chloride (Cl_inorg) is generally considered to be a hydrologically and chemically inert substance. Past research suggests that Cl_inorg participates in a complex biogeochemical cycle involving the formation of organically bound chlorine (Cl_org). The present study examines whether Cl_org cycling is sufficiently extensive as to influence the geochemical cycling of Cl_inorg. Undisturbed soil cores were collected in a coniferous forest soil in SE Sweden. The cores were stored in climate chambers for three months, irrigated with artificial rain, and the leachate was collected and analysed. The water balance of the lysimeters could be well described, and we found that 20–50% of the chlorine leached from the lysimeters was organically bound and that the amounts lost did not decrease with time. This strongly suggests that a substantial amount of Cl_org forms in topsoil, and that subsequent leaching to deeper layers causes a considerable withdrawal of Cl_inorg. The concentration of both organic carbon and Cl_org in the leachate was considerably higher than concentrations observed in the runoff in the actual catchment, suggesting that organic matter precipitates or is mineralized on its way through the soil. Copyright © 2005 John Wiley & Sons, Ltd.     

Annual fossil organic carbon delivery due to mechanical and chemical weathering of marly badlands areas

A key issue in the study of the carbon cycle is constraining the stocks and fluxes in and between C‐reservoirs. Among these, the role and importance of fossil organic carbon (FOC) release by weathering of outcropping sedimentary rocks on continental surfaces is still debated and remains poorly constrained. Our work focuses on FOC fluxes due to chemical and mechanical weathering of marls in two experimental watersheds with typical badlands geomorphology (Draix watersheds, Laval and Moulin, Alpes de Haute Provence, France). Organic matter from bedrock, soil litter and riverine particles are characterized by Rock‐Eval 6 pyrolysis. FOC fluxes due to mechanical weathering are then estimated by monitoring the annual particulate solid exports at the outlets of the watersheds (1985–2005 period). FOC fluxes from chemical weathering were calculated using Ca²⁺ concentrations in dissolved loads (year 2002) to assess the amount of FOC released by the dissolution of the carbonate matrix. Results show that FOC delivery is mainly driven by mechanical weathering, with a yield ranging from 30 to 59 t km^‐2 yr^‐1 in the Moulin (0.08 km²) and Laval (0.86 km²) catchments, respectively, (1985–2005 average). The release of FOC attributed to chemical weathering was 2.2 to 4.2 t km^‐2 for the year 2002. These high FOC fluxes from badlands are similar to those observed in tectonically active mountain catchments. At a regional scale, badland outcropping within the Durance watershed does not exceed 0.25% in area of the Rhône catchment, but could annually deliver 12 000 t yr^‐1 of FOC. This flux could correspond to 27% of the total particulate organic carbon (POC) load exported by the Rhône River to the Mediterranean Sea. At a global scale, our findings suggest that erosion of badlands may contribute significantly to the transfer of FOC from continental surfaces to depositional environments. Copyright © 2012 John Wiley & Sons, Ltd.