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1.
This paper examines the impact of contrasting antecedent soil moisture conditions on the hydrochemical response, here the changes in dissolved nitrogen (NO3?, NH4+ and dissolved organic nitrogen (DON)) and dissolved organic carbon (DOC) concentrations, of a first‐order stream during hydrological events. The study was performed in the Hermine, a 5 ha forested watershed of the Canadian Shield. It focused on a series of eight precipitation events (spring, summer and fall) sampled every 2 or 3 h and showing contrasted antecedent moisture conditions. The partition of the eight events between two groups (dry or wet) of antecedent moisture conditions was conducted using a principal component analysis (PCA). The partition was controlled (first axis explained 86% of the variability) by the antecedent streamflow, the streamflow to precipitation ratio Q/P and by the antecedent groundwater depth. The mean H+, NO3?, NH4+, total dissolved nitrogen and DOC concentrations and electrical conductivity values in the stream were significantly higher following dry antecedent conditions than after wetter conditions had prevailed in the Hermine, although the temporal variability was high (17 to 138%). At the event scale, a significantly higher proportion of the changes in DON, NO3?, and DOC concentrations in the stream was explained by temporal variations in discharge compared with the seasonal and annual scales. Two of the key hydrochemical features of the dry events were the synchronous changes in DOC and flow and the frequent negative relationships between discharge and NO3?. The DON concentrations were much less responsive than DOC to changes in discharge, whereas NH was not in phase with streamflow. During wet events, the synchronicity between streamflow and DON or NO3? was higher than during dry events and discharge and NO3? were generally positively linked. Based on these observations, the hydrological behaviour of the Hermine is conceptually compatible with a two‐component model of shallow (DON and DOC rich; variable NO3?) and deep (DON and DOC poor; variable NO3?) subsurface flow. The high NO3? and DOC levels measured at the early stages of dry events reflected the contribution from NO3?‐rich groundwaters. The contribution of rapid surface flow on water‐repellent soil materials located close to the stream channel is hypothesized to explain the DOC levels. An understanding of the complex interactions between antecedent soil moisture conditions, the presence of soil nutrients available for leaching and the dynamics of soil water flow paths during storms is essential to explain the fluxes of dissolved nitrogen and carbon in streams of forested watersheds. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
2.
Doreen Franke Michael W. Hamilton Susan E. Ziegler 《Aquatic Sciences - Research Across Boundaries》2012,74(4):751-768
Boreal watersheds contain a vast quantity of terrestrially derived dissolved organic matter (DOM) originating from wetland and forest soils, yet variation in the potential for photochemical transformation of boreal aquatic DOM sources remains poorly understood. Laboratory solar radiation exposure experiments were conducted on DOM samples collected in three seasons, across nine sites, representing contrasting catchment composition and watershed position to assess variation in the photochemical lability of boreal DOM source and stable carbon isotopic signature (δ13C) of photomineralized DOM. Dissolved organic carbon (DOC) loss rates during laboratory exposure were lowest in summer, suggesting that DOM may have been more photo-degraded during summer. DOM from upstream portions of forested stream sites and wetland-influenced sites was more photolabile relative to downstream portions and the river DOM, suggesting potential losses in photolabile DOM downstream and in the lower reaches of the watershed. Increased a254:a350 and spectral slope following sample exposure suggest photoproduction of low molecular weight (LMW) CDOM and/or a higher photoreactivity of high molecular weight versus LMW compounds. Photomineralization of nitrogen was regulated by organic nitrogen concentration and resulted in NH4 +-photoproduction rates between 0.01 and 0.3?μM N?h?1 and ecologically significant increases in NH4 + for these waters. The δ13C of the photomineralized DOM was positively correlated to initial DOC concentration and generally lower when initial DOC concentrations were lower, suggesting variation in photomineralized DOM δ13C may be a result of kinetic isotope fractionation. Results from this study demonstrate significant variation in the photochemical lability of boreal watershed sources of DOM. Such variation suggests landscape and environmental change has the potential to alter the biogeochemical role photochemical transformations play in downstream portions of boreal watersheds. 相似文献
3.
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. 相似文献
4.
Frantisek Buzek Martin Novak Bohuslava Cejkova Ivana Jackova Jan Curik Frantisek Veselovsky Marketa Stepanova Eva Prechova Leona Bohdalkova 《水文研究》2019,33(21):2792-2803
Dissolved organic carbon (DOC) originating in peatlands can be mineralized to carbon dioxide (CO2) and methane (CH4), two potent greenhouse gases. Knowledge of the dynamics of DOC export via run‐off is needed for a more robust quantification of C cycling in peatland ecosystems, a prerequisite for realistic predictions of future climate change. We studied dispersion pathways of DOC in a mountain‐top peat bog in the Czech Republic (Central Europe), using a dual isotope approach. Although δ13CDOC values made it possible to link exported DOC with its within‐bog source, δ18OH2O values of precipitation and run‐off helped to understand run‐off generation. Our 2‐year DOC–H2O isotope monitoring was complemented by a laboratory peat incubation study generating an experimental time series of δ13CDOC values. DOC concentrations in run‐off during high‐flow periods were 20–30 mg L?1. The top 2 cm of the peat profile, composed of decaying green moss, contained isotopically lighter C than deeper peat, and this isotopically light C was present in run‐off in high‐flow periods. In contrast, baseflow contained only 2–10 mg DOC L?1, and its more variable C isotope composition intermittently fingerprinted deeper peat. DOC in run‐off occasionally contained isotopically extremely light C whose source in solid peat substrate was not identified. Pre‐event water made up on average 60% of the water run‐off flux, whereas direct precipitation contributed 40%. Run‐off response to precipitation was relatively fast. A highly leached horizon was identified in shallow catotelm. This peat layer was likely affected by a lateral influx of precipitation. Within 36 days of laboratory incubation, isotopically heavy DOC that had been initially released from the peat was replaced by isotopically lighter DOC, whose δ13C values converged to the solid substrate and natural run‐off. We suggest that δ13C systematics can be useful in identification of vertically stratified within‐bog DOC sources for peatland run‐off. 相似文献
5.
Factors controlling nitrogen and dissolved organic carbon exports across timescales in two watersheds with different land uses
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Rui Jiang Ryusuke Hatano Ying Zhao Kanta Kuramochi Atsushi Hayakawa Krishna P. Woli Mariko Shimizu 《水文研究》2014,28(19):5105-5121
Investigating factors controlling the temporal patterns of nitrogen (N) and dissolved organic carbon (DOC) exports on the basis of a comparative study of different land uses is beneficial for managing water resources, especially in agricultural watersheds. We focused our research on an agricultural watershed (AW) and a forested watershed (FW) located in the Shibetsu watershed of eastern Hokkaido, Japan, to investigate the temporal patterns of N and DOC exports and factors controlling those patterns at different timescales (inter‐annual, seasonal, and hydrological event scales). Results showed that the annual patterns of N and DOC exports significantly varied over time and were probably controlled by climate. Higher discharge volumes in 2003, a wet year, showed higher N and DOC loadings in both watersheds. However, this process was also regulated by land use associated with N inputs. Higher concentrations and loadings were shown in the agricultural watershed. At the seasonal scale, N and DOC exports in the AW and the FW were more likely controlled by sources associated with land use. The Total N (TN) and Nitrate‐N (NO3?‐N) had higher concentrations during snowmelt season in the AW, which may be attributed to manure application in late autumn or early winter in the agricultural watershed. Concentrations of TN, NO3?‐N, dissolved organic nitrogen (DON), and DOC showed higher values during the summer rainy season in the FW, related to higher litter decomposition during summer and autumn and the fertilizer application in the agricultural area during summer. Higher DOC concentrations and loadings were observed during the rainy season in the AW, which is probably attributed to higher DOC production related to temperature and microbial activity during summer and autumn in grasslands. Correlations between discharge and concentrations differed during different periods or in different watersheds, suggesting that weather discharge can adequately represent the fact that N export depends on N concentrations, discharge level, and other factors. The differing correlations between N/DOC concentrations and the Si concentration indicated that the N/DOC exports might occur along different flow paths during different periods. During baseflow, the high NO3?‐N exports were probably derived from deep groundwater and might have percolated from uplands during hydrological events. During hydrological events, NO3?‐N exports may occur along near‐surface flow paths and in deep groundwater, whereas DOC exports could be related to near‐surface flow paths. At the event scale, the relationships between discharge and concentrations of N and DOC were regulated by antecedent soil moisture (shallow groundwater condition) in each watershed. These results indicated that factors controlling N and DOC exports varied at different timescales in the Shibetsu area and that better management of manure application during winter in agricultural lands is urgently needed to control water pollution in streams. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
6.
We studied the relationships between streamwater chemistry and the topography of subcatchments in the Dorokawa watershed in Hokkaido Island, northern Japan, to examine the use of topography as a predictor of streamwater chemistry in a watershed with relatively moderate terrain compared with other regions of Japan. Topographic characteristics of the Dorokawa watershed and its subcatchments were expressed as topographic index (TI) values, which ranged from 4·5 to 20·4 for individual grid cells (50 × 50 m2), but averaged from 6·4 to 7·4 for the 20 subcatchments. Streamwater samples for chemical analyses were collected four times between June and October 2002 from 20 locations in the watershed. The pH of water that passed through the watershed increased from ~5·0 to 7·0, with major increases in Na+ and Ca2+ and marked decreases in NO3? and SO . Distinctive spatial patterns were observed for dissolved organic carbon (DOC), dissolved organic nitrogen (DON), and NO3? concentrations of streamwater across the watershed. Statistical analyses indicated significant linear relationships between the average TI values of subcatchments and DOC, DON, and NO3? concentrations. Furthermore, the proportion of DOC in streamwaters in the wet season increased with TI values relative to other nitrogen species, whereas NO3? concentrations decreased with TI. The gradients of soil wetness and the presence of wetlands explained many of the observed spatial and temporal patterns of DOC, DON, and NO3? concentrations in the surface waters of the Dorokawa watershed. Our results suggest that the TI is especially useful for predicting the spatial distribution of DOC, DON and NO3? in the surface waters of Hokkaido, where topographical relief is moderate and wetlands more common than in other regions of Japan. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
7.
The changes of NH3-N, NO3-N, NO2-N and TN/TP were studied during growth and non-growth season in 33 subtropical shallow lakes in the middle and lower reaches of the Yangtze River. There were significant positive correlations among all nutrient concentrations, and the correlations were better in growth season than in non-growth season. When TP>0.1 mgL?1, NH3-N increased sharply in non-growth season with increasing TP, and NO3-N increased in growth season but decreased in non-growth season with TP. These might be attributed to lower dissolved oxygen and low temperature in non-growth season of the hypereutrophic lakes, since nitrification is more sensitive to dissolved oxygen and temperature than antinitrification. When 0.1 mgL?1>TP>0.035 mgL?1, TN and all kinds of inorganic nitrogen were lower in growth season than in non-growth season, and phytoplankton might be the vital regulating factor. When TP<0.035 mgL?1, inorganic nitrogen concentrations were relatively low and NH3-N, NO2-N had significant correlations with phytoplankton, indicating that NH3-N and NO2-N might be limiting factors to phytoplankton. In addition, TN/TP went down with decline in TP concentration, and TN and inorganic nitrogen concentrations were obviously lower in growth season than in non-growth season, suggesting that decreasing nitrogen (especially NH3-N and NO3-N) was an important reason for the decreasing TN/TP in growth season. The ranges of TN/TP were closely related to trophic level in both growth and non-growth seasons, and it is apparent that in the eutrophic and hypertrophic state the TN/TP ratio was obviously lower in growth season than in non-growth season. The changes of the TN/TP ratio were closely correlated with trophic levels, and both declines of TN in the water column and TP release from the sediment were important factors for the decline of the TN/TP ratio in growth season. 相似文献
8.
Entrapped gas bubbles in peat can alter the buoyancy, storativity, void ratio and expansion/contraction properties of the peat. Moreover, when gas bubbles block water‐conducting pores they can significantly reduce saturated hydraulic conductivity and create zones of over‐pressuring, perhaps leading to an alteration in the magnitude and direction of groundwater flow and solute transport. Some previous researches have demonstrated that these zones of over‐pressuring are not observed by the measurements of pore‐water pressures using open‐pipe piezometers in peat; rather, they are only observed with pressure transducers sealed in the peat. In has been hypothesized that open‐pipe piezometers vent entrapped CH4 to the atmosphere and thereby do not permit the natural development of zones of entrapped gas. Here we present findings of the study to investigate whether piezometers vent subsurface CH4 to the atmosphere and whether the presence of piezometers alters the subsurface concentration of dissolved CH4. We measured the flux of methane venting from the piezometers and also determined changes in pore‐water CH4 concentration at a rich fen in southern Ontario and a poor fen in southern Quebec, in the summer of 2004. Seasonally averaged CH4 flux from piezometers was 1450 and 37·8‐mg CH4 m?2 d?1 at the southern Ontario site and Quebec site, respectively. The flux at the Ontario site was two orders of magnitude greater than the diffusive flux at the site. CH4 pore‐water concentrations were significantly lower in open piezometers than in water taken from sealed samplers at both the Ontario and Quebec sites. The flux of CH4 from piezometers decreased throughout the season suggesting that CH4 venting through the piezometer exceeded the rate of methanogenesis in the peat. Consequently we conclude that piezometers may alter the gas dynamics of some peatlands. We suggest that less‐invasive techniques (e.g. buried pressure transducers, tracer experiments) are needed for the accurate measurement of pore‐water pressures and hydraulic conductivity in peatlands with a large entrapped gas component. Furthermore, we argue that caution must be made in interpreting results from previous peatland hydrology studies that use these traditional methods. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
9.
This study analysed the importance of precipitation events from May 2003 to April 2004 on surface water chemistry and solute export from a 696 ha glaciated forested watershed in western New York State, USA. The specific objectives of the study were to determine: (a) the temporal patterns of solutes within individual storm events; (b) the impact of precipitation events on seasonal and annual export budgets; and (c) how solute concentrations and loads varied for precipitation events among seasons as functions of storm intensity and antecedent moisture conditions. Analysis of solute trajectories showed that NH4+, total Al and dissolved organic nitrogen (DON) peaked on the hydrograph rising limb, whereas dissolved organic carbon (DOC) concentrations peaked following the discharge peak. Sulphate and base‐cations displayed a dilution pattern with a minimum around peak discharge. End‐member mixing analysis showed that throughfall contributions were highest on the rising limb, whereas valley‐bottom riparian waters peaked following the discharge peak. The trajectories of NO3? concentrations varied with season, indicating the influence of biotic processes on the generation, and hence flux, of this solute. Storm events had the greatest impact on the annual budgets for NH4+, K+, total dissolved Al, DON and DOC. Storm events during summer had the greatest impact on seasonal solute budgets. Summer events had the highest hourly discharges and high concentrations of solutes. However, NO3? and DOC exports during a spring snowmelt event were considerably more than those observed for large events during other periods of the year. Comparisons among storms showed that season, precipitation amount, and antecedent moisture conditions affected solute concentrations and loads. Concentrations of solutes were elevated for storms that occurred after dry antecedent conditions. Seven of the largest storms accounted for only 15% of the annual discharge, but were responsible for 34%, 19%, 64%, 13%, 39% and 24% of the annual exports of NH4+, K+, Al, NO3?, DON and DOC respectively. These results suggest that the intense and infrequent storms predicted for future climate‐change scenarios will likely increase the exports of solutes like DOC, DON, NH4+, Al and K+ from watersheds. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
10.
以太湖重度蓝藻水华发生的西北湖区为研究对象,从河口至湖心区设置5个采样点,于2012年10月至2013年10月逐月采集表层水体样品,测定了水温、溶解氧和浮游细菌丰度,并分析了浮游植物群落结构的组成、溶解性无机氮(DIN)和有机氮(DON)浓度以及氮磷比.研究结果表明,太湖西北湖区浮游植物主要由蓝藻、硅藻、绿藻和隐藻组成.可能由于风、浪等混合作用使太湖西北湖区不同采样点之间蓝藻细胞密度没有显著差异.蓝藻生物量在浮游植物中所占比例最高为34%±15%,春季部分点位隐藻生物量高于50%,表明隐藻与蓝藻的相互竞争趋势显著.CCA排序图结果表明,DIN、DON浓度以及总氮∶总磷比(TN∶TP比)是影响西北湖区浮游植物优势属分布的重要环境因子.5个采样点铵态氮(NH_4~+-N)与DIN浓度具有显著差异,与DON浓度没有显著差异.夏季蓝藻水华暴发期间,可能由于蓝藻的吸收利用引起NH_4~+-N和硝态氮(NO_3~--N)浓度迅速降低.此外,由于NH_4~+-N浓度还可能受到沉积物NH_4~+-N释放的影响,因此,蓝藻细胞密度与NO_3~--N的相关系数和显著水平均高于NH_4~+-N.夏季TN∶TP比和DIN∶TP比降至最低,表明该湖区浮游植物,尤其是蓝藻的生长可能受到氮限制.蓝藻细胞密度与DON浓度呈显著负相关,表明在氮限制条件下,DON可能是蓝藻氮素利用的重要补充. 相似文献
11.
Alan R. Hill 《水文研究》2012,26(20):3135-3146
The effect of preferential flow in soil pipes on nitrate retention in riparian zones is poorly understood. The characteristics of soil pipes and their influence on patterns of groundwater transport and nitrate dynamics were studied along four transects in a 1‐ to >3‐m deep layer of peat and marl overlying an oxic sand aquifer in a riparian zone in southern Ontario, Canada. The peat‐marl deposit, which consisted of several horizontal layers with large differences in bulk density, contained soil pipes that were generally 0.1 to 0.2 m in diameter and often extended vertically for 1 to >2 m. Springs that produced overland flow across the riparian area occurred at some sites where pipes extended to the peat surface. Concentrations of NO3?–N (20–30 mg L?1) and dissolved oxygen (DO) (4–6 mg L?1) observed in peat pipe systems and surface springs were similar to values in the underlying sand aquifer, indicating that preferential flow transported groundwater with limited nitrate depletion. Low NO3?–N concentrations of <5 mg L?1 and enriched δ15N values indicated that denitrification was restricted to small areas of the peat where pipes were absent. Groundwater DO concentrations declined rapidly to <2 mg L?1 in the peat matrix adjacent to pipes, whereas high NO3?–N concentrations of >15 mg L?1 extended over a larger zone. Low dissolved organic carbon values at these locations suggest that supplies of organic carbon were not sufficient to support high rates of denitrification, despite low DO conditions. These data indicate that it is important to develop a greater understanding of pipes in peat deposits, which function as sites where the transport of large fluxes of water with low biogeochemical reaction rates can limit the nitrate removal capacity of riparian zones. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
12.
Ian C. Grieve 《地球表面变化过程与地形》1985,10(1):75-78
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. 相似文献
13.
The sandy littoral zone of Lake Tegel (Berlin, Germany) was investigated during 2004–2006 down to sediment depths ≥26 cm to derive a scheme of seasonal carbon turnover under induced bank filtration conditions. Carbon turnover processes were quantified regarding external and internal sources of dissolved and particulate organic matter (DOM and POM), primary production, community respiration, redox potential as well as specific loads of soluble chemical compounds such as nitrogen, iron, manganese and DOC.Over the course of the year, infiltrating DOC decreased by about 13–20% within the upper 26 cm sediment of the infiltration stretch. Gradients of all observed soluble compounds that are highly cross-linked to biological activities were highest in the topmost centimetre. In this depth mass balances (output–input) were negative concerning NO3-N (−1 mg dm−2 d−1, summer mean) and DOC (−2 mg dm−2 d−1, winter mean), respectively, while specific loads of cations such as manganese reached up to 0.2 mg dm−2 d−1 during summer. Carbon mineralization ranged between 3 and 7 mg C dm−2 d−1 and was nearly twice as high in summer as in winter. The turnover of the infiltrating DOC contributed maximally 25% in summer to 50% in winter to the entire organic carbon mineralization. Gross and net primary production differed up to a factor of >10, indicating very fast turnover reactions and the predominance of community respiration and mineralization, respectively. The POC in the upper sediment layer (10 cm) temporally varied around 1% sediment d.w.; benthic algae, organic seston input and autumnal leaf fall contributed similar percentages to the POC pool. 相似文献
14.
Mari Ito Myron J. Mitchell Charles T. Driscoll Robert M. Newton Chris E. Johnson Karen M. Roy 《水文研究》2007,21(10):1249-1264
The southwestern Adirondack region of New York receives among the highest rates of atmospheric nitrogen (N) deposition in the USA. Atmospheric N deposition to sensitive ecosystems, like the Adirondacks, may increase the acidification of soils through losses of exchangeable nutrient cations, and the acidification of surface waters associated with enhanced mobility of nitrate (NO3?). However, watershed attributes, including surficial terrestrial characteristics, in‐lake processing, and geological settings, have been found to complicate the relationships between atmospheric N deposition and N drainage losses. We studied two lake‐watersheds in the southwestern Adirondacks, Grass Pond and Constable Pond, which are located in close proximity (~26 km) and receive similarly high N deposition, but have contrasting watershed attributes (e.g. wetland area, geological settings). Since the difference in the influence of N deposition was minimal, we were able to examine both within‐ and between‐watershed influences of land cover, the contribution of glacial till groundwater inputs, and in‐lake processes on surface water chemistry with particular emphasis on N solutes and dissolved organic carbon (DOC). Monthly samples at seven inlets and one outlet of each lake were collected from May to October in 1999 and 2000. The concentrations of NO3? were high at the Grass Pond inlets, especially at two inlets, and NO3? was the major N solute at the Grass Pond inlets. The concentrations of likely weathering products (i.e. dissolved Si, Ca2+, Mg2+, Na+) as well as acid neutralizing capacity and pH values, were also particularly high at those two Grass Pond inlets, suggesting a large contribution of groundwater inputs. Dissolved organic N (DON) was the major N solute at the Constable Pond inlets. The higher concentrations of DON and DOC at the Constable Pond inlets were attributed to a large wetland area in the watershed. The DOC/DON ratios were also higher at the Constable Pond inlets, possibly due to a larger proportion of coniferous forest area. Although DON and DOC were strongly related, the stronger relationship of the proportion of wetland area with DOC suggests that additional factors regulate DON. The aggregated representation of watershed physical features (i.e. elevation, watershed area, mean topographic index, hypsometric‐analysis index) was not clearly related to the lake N and DOC chemistry. Despite distinctive differences in inlet N chemistry, NO3? and DON concentrations at the outlets of the two lakes were similar. The lower DOC/DON ratios at the lake outlets and at the inlets having upstream ponds suggest the importance of N processing and organic N sources within the lakes. Although an inverse relationship between NO3? and DOC/DON has been suggested to be indicative of a N deposition gradient, the existence of this relationship for sites that receive similar atmospheric N deposition suggest that the relationship between NO3? and the DOC/DON ratio is derived from environmental and physical factors. Our results suggest that, despite similar wet N deposition at the two watershed sites, N solutes entering lakes were strongly affected by hydrology associated with groundwater contribution and the presence of wetlands, whereas N solutes leaving lakes were strongly influenced by in‐lake processing. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
15.
《Limnologica》2019
This study aimed to evaluate the importance of physical, chemical and biological factors (e.g., chlorophyll-a, and carbon) in the regulation of the summer epilimnion thickness (Zmix) of the tropical lakes focusing on trends of the current environmental variability. We sampled a set of tropical lakes from the middle Rio Doce lacustrine system (Minas Gerais, Brazil) for two consecutive summers. Besides Zmix, we analyzed the visible light attenuation (KdPAR), dissolved organic carbon (DOC), chlorophyll-a (Chl-a), total suspended solids (TSS), and fetch. We also analyze the quality of the dissolved organic matter (DOM) through colored dissolved organic matter (CDOM), spectral slope (S), DOC-specific absorbance (SUVA) and the ratio between the absorbance at 250 nm and 365 nm (E250:365). Our results showed quite different results during the two years studied. In the summer of 2012, when there was higher rainfall, variations in Zmix were correlated to the optical factors associated with DOM quality, while in the drier summer of 2013 Chl-a, TSS and fetch were the variables that more explained Zmix. It suggests that DOM regulates the Zmix in the rainy periods in the studied tropical lakes and that control is determined by the balance between the DOM input (runoff) and output (such as photodegradation) of the aquatic systems. In reduced rain conditions (summer 2013), the factors responsible by chemistry photodegradation of DOM were predominant, and the organic matter was no longer controlling Zmix, which was driven by internal mixing, productivity, and the wind (Chl-a, TSS and fetch). In this study we showed how changes in precipitation might cause shifts in the factors that regulate the epilimnion thickness in tropical lakes. 相似文献
16.
Spectroscopic techniques and extracellular enzyme activity measurements were combined with assessments of bacterial secondary production (BSP) to elucidate flood-pulse-linked differences in carbon (C) sources and related microbial processes in a river-floodplain system near Vienna (Austria). Surface connection with the main channel significantly influenced the quantity and quality of dissolved organic matter (DOM) in floodplain backwaters. The highest values of dissolved organic carbon (DOC) and chromophoric DOM (CDOM) were observed during the peak of the flood, when DOC increased from 1.36 to 4.37 mg l?1 and CDOM from 2.94 to 14.32 m?1. The flood introduced DOC which consisted of more allochthonously-derived, aromatic compounds. Bacterial enzymatic activity, as a proxy to track the response to changes in DOM, indicated elevated utilization of imported allochthonous material. Based on the enzyme measurements, new parameters were calculated: metabolic effort and enzymatic indices (EEA 1 and EEA 2). During connection, bacterial glucosidase and protease activity were dominant, whereas during disconnected phases a switch to lignin degradation (phenol oxidase) occurred. The enzymatic activity analysis revealed that flooding mobilized reactive DOM, which then supported bacterial metabolism. No significant differences in overall BSP between the two phases were detected, indicating that heterogeneous sources of C sufficiently support BSP. The study demonstrates that floods are important for delivering DOM, which, despite its allochthonous origin, is reactive and can be effectively utilized by aquatic bacteria in this river-floodplain systems. The presence of active floodplains, characterized by hydrological connectivity with the main channel, creates the opportunity to process allochthonous DOC. This has potential consequences for carbon flux, enhancing C sequestration and mineralization processes in this river-floodplain system. 相似文献
17.
本研究在太湖梅梁湾采集沉积柱,采用一种自制的毫米级柱状沉积物自动垂向分层切割装置对表层50 mm沉积物进行垂向切割(间隔2 mm),结合高通量测序技术分析沉积物中细菌群落的毫米级垂向分布;同时采用毫米级高分辨透析技术和薄膜扩散梯度技术(DGT)分析溶解态和DGT可获取态铵态氮(NH4+-N)、硝态氮(NO3--N)、Fe、P的垂向分布特征。结果显示,沉积物中细菌群落与溶解态和DGT可获取态氮铁磷浓度在垂向上呈现显著的异质性。细菌硝酸盐还原主要发生在-16~0 mm沉积物深度,这可能导致了溶解态和DGT可获取态NO3--N含量在该沉积物深度的明显减少。细菌铁还原主要分布在-32~-18 mm沉积物深度,细菌硫酸盐还原主要分布在-50~-34 mm的沉积物深度;细菌硫酸盐还原是导致沉积物溶解态和DGT可获取态铁磷浓度从-32 mm随沉积物的深度增加而显著增加的主要原因。本研究加深了对富营养化湖泊沉积物中细菌影响氮磷在垂向上迁移转化的认识。 相似文献
18.
This study examines the release of dissolved organic carbon (DOC) from upland peat during the period of the autumn flushing. Hydroclimatic conditions were monitored in conjunction with measurements of absorbance and the E4/E6 ratio of the stream draining an 11·4 km2 upland peat catchment in northern England. During two months of monitoring the effects of 67 separate rainfall events were examined showing that:
- The peat behaves hydrologically as if it were a two end‐member system consisting of old, interevent, and new, event, water. Runoff is initiated by percolation excess of new water at the acrotelm–catotelm interface.
- The discharge of dissolved organic matter behaves like a three end‐member system with the between‐event water being low in DOC and storm events being characterized by two types of water. Initial runoff being characterized by new water rich in DOC that gives way to new water depleted in DOC. This transition can be ascribed to the runoff progressing from throughflow within the acrotelm progressing to saturation‐excess overland flow.
- Depletion of DOC during storm events is accompanied by a change in the character of the DOC as the E4/E6 ratio changes. This suggests that the decrease in DOC during events is the result of exhaustion of reserves rather than changes in the flowpaths being utilized by runoff.
- The amount of carbon released in any event is critically dependent upon the time between events during which oxidation processes generate a reservoir of available carbon. Production of available carbon in the catchment is as high as 4·5 g C per day per m3 of peat, suggesting a turnover rate of peat of the order of 42 years. Copyright © 2002 John Wiley & Sons, Ltd.
19.
Searching for similarity in topographic controls on carbon,nitrogen and phosphorus export from forested headwater catchments 总被引:1,自引:0,他引:1
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Samson G. Mengistu Irena F. Creed Kara L. Webster Eric Enanga Frederick D. Beall 《水文研究》2014,28(8):3201-3216
Topography influences hydrological processes that in turn affect biogeochemical export to surface water on forested landscapes. The differences in long‐term average annual dissolved organic carbon (DOC), organic and inorganic nitrogen [NO3?‐N, dissolved organic nitrogen (DON)], and phosphorus (total dissolved phosphorus, TDP) export from catchments in the Algoma Highlands of Ontario, Canada, with similar climate, geology, forest and soil were established. Topographic indicators were designed to represent topographically regulated hydrological processes that influence nutrient export, including (1) hydrological storage potential (i.e. effects of topographic flats/depressions on water storage) and (2) hydrological flushing potential (i.e. effects of topographic slopes on potential for variable source area to expand and tap into previously untapped areas). Variations in NO3?‐N export among catchments could be explained by indicators representing both hydrological flushing potential (91%, p < 0.001) and hydrological storage potential (65%, p < 0.001), suggesting the importance of hydrological flushing in regulating NO3?‐N export as well as surface saturated areas in intercepting NO3?‐N‐loaded runoff. In contrast, hydrological storage potential explained the majority of variations among catchments in DON (69%, p < 0.001), DOC (94%, p < 0.001) and TDP (82%, p < 0.001) export. The lower explanatory power of DON (about 15% less) compared with that of DOC and TDP suggests another mechanism influencing N export, such as controls related to alternative fates of nitrogen (e.g. as gas). This study shows that simple topographic indicators can be used to track nutrient sources, sinks and their transport and export to surface water from catchments on forest landscapes. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
20.
湖光岩玛珥湖水体中营养盐的时空分布特征及其影响因素 总被引:1,自引:0,他引:1
湖光岩玛珥湖是世界上最大的玛珥湖,它几乎是封闭的,受外界的干扰小.目前有关玛珥湖的研究主要集中在古气候及生态环境研究方面,而有关玛珥湖营养盐在一年中的生物地球化学循环的研究较少,因此研究湖光岩玛珥湖营养盐的生物地球化学过程具有重要意义.于2015年10月-2016年9月对湖光岩玛珥湖全水柱的营养盐及其他相关参数进行逐月调查,分析营养盐的结构特征、垂直分布特征和时间变化情况,并讨论营养盐时空变化的影响因素.结果表明,湖光岩玛珥湖水中的无机氮(DIN)以铵态氮(NH4+-N)为主(>60%),其次是硝态氧(NO3--N),亚硝态氮(NO2--N)所占比利最低.湖光岩玛珥湖水中的硅酸盐(SiO32--Si)浓度较高,水体浮游植物生长受磷限制.冬季风期间,水体垂直混合较均匀,导致营养盐的垂直分布比较均匀;夏季风期间,水体层化,营养盐浓度在浅层水体较低,在深层水体较高.湖光岩玛珥湖表层水中的NO3--N、NH4+-N和SiO32--Si具有明显的时间变化规律:NO3--N浓度从10月-次年3月升高,从3-9月降低;NH4+-N浓度从10月-次年5月降低;SiO32--Si浓度从11月-次年5月降低,从5-9月持续升高.营养盐浓度的时间变化受有机质的矿化分解、水体的季节性混合、浮游植物的吸收、降雨的输入等多种因素的综合影响. 相似文献