ABSTRACT
Dissimilatory iron reduction (DIR) can drive the release of organic carbon (OC) as carbon dioxide (CO2 ) by mediating electron transfer between organic compounds and microbes. However, DIR is also crucial for carbon sequestration, which can affect inorganic-carbon redistribution via iron abiotic-phase transformation. The formation conditions of modern carbonate-bearing iron minerals (ICFe ) and their potential as a CO2 sink are still unclear. A natural environment with modern ICFe , such as karst lake sediment, could be a good analog to explore the regulation of microbial iron reduction and sequential mineral formation. We find that high porosity is conducive to electron transport and dissimilatory iron-reducing bacteria activity, which can increase the iron reduction rate. The iron-rich environment with high calcium and OC can form a large sediment pore structure to support rapid DIR, which is conducive to the formation and growth of ICFe . Our results further demonstrate that the minimum DIR threshold suitable for ICFe formation is 6.65 µmol g-1 dw day-1 . DIR is the dominant pathway (average 66.93%) of organic anaerobic mineralization, and the abiotic-phase transformation of Fe2+ reduces CO2 emissions by ~41.79%. Our findings indicate that as part of the carbon cycle, DIR not only drives mineralization reactions but also traps carbon, increasing the stability of carbon sinks. Considering the wide geographic distribution of DIR and ICFe , our findings suggest that the "iron mesh" effect may become an increasingly important vector of carbon sequestration.
Subject(s)
Carbon Sequestration , Iron , Iron/chemistry , Iron/metabolism , Carbon Dioxide , Oxidation-Reduction , Carbon Cycle , Ferric Compounds/metabolismABSTRACT
Dissolved organic matter (DOM) is a heterogeneous pool of compounds and exhibits diverse adsorption characteristics with or without phosphorous (P) competition. The impacts of these factors on the burial and mobilization of organic carbon and P in aquatic ecosystems remain uncertain. In this study, an algae-derived DOM (ADOM) and a commercially available humic acid (HA) with distinct compositions were assessed for their adsorption behaviors onto iron (oxy)hydroxides (FeOx), both in the absence and presence of phosphate. ADOM contained less aromatics but more protein-like and highly unsaturated structures with oxygen compounds (HUSO) than HA. The adsorption capacity of FeOx was significantly greater for ADOM than for HA. Protein-like and HUSO compounds in ADOM and humic-like compounds and macromolecular aromatics in HA were preferentially adsorbed by FeOx. Moreover, ADOM demonstrated a stronger inhibitory effect on phosphate adsorption than HA. This observation suggests that the substantial release of autochthonous ADOM by algae could elevate internal P loading and pose challenges for the restoration of restore eutrophic lakes. The presence of phosphate suppressed the adsorption of protein-like compounds in ADOM onto FeOx, resulting in an increase in the relative abundance of protein-like compounds and a decrease in the relative abundance of humic-like compounds in post-adsorption ADOM. In contrast, phosphate exhibited no discernible impact on the compositional fractionation of HA. Collectively, our results show the source-composition characters of DOM influence the immobilization of both DOM and P in aquatic ecosystems through adsorption processes. The preferential adsorption of proteinaceous compounds within ADOM and aromatics within HA highlights the potential for the attachment with FeOx to diminish the original source-specific signatures of DOM, thereby contributing to the shared DOM characteristics observed across diverse aquatic environments.
Subject(s)
Carbon , Ferric Compounds , Humic Substances , Lakes , Phosphates , Phosphorus , Water Pollutants, Chemical , Adsorption , Phosphorus/chemistry , Lakes/chemistry , Phosphates/chemistry , Humic Substances/analysis , Water Pollutants, Chemical/chemistry , Carbon/chemistry , Ferric Compounds/chemistry , Models, ChemicalABSTRACT
Alpine lake habitats are evolving into subalpine lakes under the scenario of climate change, where the vegetation are promoted due to increasing temperature and precipitation. The abundant terrestrial dissolved organic matter (TDOM) leached from watershed soil into subalpine lakes would undergo strong photochemical reaction due to the high altitude, with the potential to alter DOM composition and affect the bacterial communities. To reveal the transformation of TDOM by both photochemical and microbial processes in a typical subalpine lake, Lake Tiancai (located 200 m below the tree line) was chosen. TDOM was extracted from the surrounding soil of Lake Tiancai and then subjected to the photo/micro-processing for 107 days. The transformation of TDOM was analyzed by Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR MS) and fluorescence spectroscopy, and the shift of bacterial communities was analyzed using 16s rRNA gene sequencing technology. Dissolved organic carbon and light-absorbing components (a350) decay accounted for approximately 40% and 80% of the original, respectively, in the sunlight process, but both less than 20% in the microbial process for 107 days. The photochemical process promoted the chemodiversity as there were â¼7000 molecules after sunlight irradiation, compared to â¼3000 molecules in the original TDOM. Light promoted the production of highly unsaturated molecules and aliphatics, which were significantly associated with Bacteroidota, suggesting that light may influence bacterial communities by regulating the DOM molecules. Carboxylic-rich alicyclic molecules were generated in both photochemical and biological processes, suggesting TDOM was converted to a stable pool over time. Our finding on the transformation of terrestrial DOM and the alternation of bacterial community under the simultaneously photochemical and microbial processes will help to reveal the response of the carbon cycle and lake system structure to climate change for high-altitude lakes.
Subject(s)
Lakes , Sunlight , Lakes/chemistry , RNA, Ribosomal, 16S/genetics , Bacteria/genetics , Soil , BiodiversityABSTRACT
The light-to-nutrient hypothesis proposes that under high light-to-nutrient conditions, bacteria tend to be limited by phosphorus (P), while under relatively low light-to-nutrient conditions, bacteria are likely driven towards carbon (C) limitation. Exploring whether this light-to-nutrient hypothesis is fitting for alpine lakes has profound implications for predicting the impacts of climatic and environmental changes on the structures and processes of aquatic ecosystems in climate-sensitive regions. We investigated the environmental conditions and bacterioplankton community compositions of 15 high-elevation lakes (7 above and 8 below treeline). High light-to-nutrient conditions (denoted by the reciprocal value of the attenuation coefficient (1/K) to total phosphorus (TP)), high chlorophyll a (Chl a) concentrations, low TP concentrations and low ratios of the dissolved organic carbon concentration to the dissolved total nitrogen concentration (DOC:DTN) were detected in above-treeline lakes. Significant positive correlations between the bacterioplankton community compositions with 1/K:TP ratios and Chl a concentrations indicated that not only high light energy but also nutrient competition between phytoplankton and bacteria could induce P limitation for bacteria. In contrast, low light-to-nutrient conditions and high allochthonous DOC input in below-treeline lakes lessen P limitation and C limitation. The most abundant genus, Polynucleobacter, was significantly enriched, and more diverse oligotypes of Polynucleobacter operational taxonomic units were identified in the below-treeline lakes, indicating the divergence of niche adaptations among Polynucleobacter oligotypes. The discrepancies in the light-to-P ratio and the components of organic matter between the above-treeline and below-treeline lakes have important implications for the nutrient limitation of bacterioplankton and their community compositions.
Subject(s)
Ecosystem , Lakes , Bacteria , Chlorophyll A , Lakes/chemistry , Nitrogen , Nutrients , PhosphorusABSTRACT
Color dissolved organic matter (CDOM) plays a key role in lacustrine ecosystems and its composition is commonly mediated by the allochthonous input and autochthonous production. Deep lakes have a strong in-lake processing, which highly affects the sources, composition and cycle of CDOM. Here, the second deepest lake (Lake Fuxian) in China was selected to investigate the effects of allochthonous input and in-lake processing on lacustrine CDOM in deep lakes. Firstly, a detailed survey on CDOM composition across Lake Fuxian in the top water layer and inflowing rivers was carried out in the wet season representing the allochthonous input. In addition, CDOM in Lake Fuxian was compared with those in other lakes with distinct catchment characteristics and lake morphology. The results showed that compared to lacustrine CDOM in Lake Fuxian, the riverine CDOM contained much more humic-like substances, resulting in the humic-like fluorescence intensity peaked at the confluence of rivers into Lake Fuxian. In contrast, CDOM in Lake Fuxian was dominated by the protein-like substance. Comparison of CDOM composition among Lake Fuxian (well-vegetated catchment, deep lakes) with other diverse lakes in China (shallow/deep lakes with poor-vegetated catchment, and shallow lakes with well-vegetated catchment) showed similar CDOM quality in all type lakes, which were dominated by non-humified and autochthonous CDOM. Yet, CDOM quantity increased as the orders of deep lakes within poor-vegetated (Tibetan deep lakes) < the deep lake within well-vegetated catchment (Lake Fuxian) < shallow lakes within poorly-vegetated catchment (Tibetan shallow lakes) < shallow lakes within well-vegetated catchment (lakes along the middle and lower reaches of Yangtze River). Our results evidenced that the effect of allochthonous input on CDOM composition could be counteracted by in-lake processing in deep lakes. For deep lakes, a comprehensive understanding of in-lake processing of CDOM is critical for predicting lacustrine DOM composition and cycle.
Subject(s)
Dissolved Organic Matter , Lakes , Ecosystem , Rivers , Humic Substances/analysis , China , Spectrometry, FluorescenceABSTRACT
The stability of organic matter-iron-phosphate (OM-Fe-P) association has an important impact on the migration and sequestration of organic carbon (OC) and P in the environment. Here, we examined the release characteristics of Fe, P and OM due to the abiotic reduction of OM-Fe-P associations by Na-dithionite. The associations were synthesized with algae-derived OM (AOM) and terrestrial humic acid (HA) through either adsorption onto iron (hydr)oxide or coprecipitation with Fe(III). Results indicated that OM and P adsorbed onto the associations were rapidly released, whereas coprecipitation yielded much lower release rates of Fe, P, and OM. The stronger inhibitory effect on reduction from coprecipitation can be explained by larger particles formed by coprecipitation and coprecipitation taking up more OC that had a passivation effect on the associations. The release rates of OM and P were lower in coprecipitates formed with HA than formed with AOM for a given OC/Fe ratio. This observation can be attributed to a patchy distribution of OC in AOM associated coprecipitates, which showed a weaker aggregation of OC with Fe and P. In contrast, the distribution of OC in HA-associated coprecipitates was more homogenous, enabling a stronger aggregation of OM with P and a greater passivation effect on P release. Our results revealed that OM sources, association formation pathways, and elemental stoichiometry collectively controlled the stability of OM-Fe-P associations.
ABSTRACT
Algal-dissolved organic matter (ADOM) is an important fraction of dissolved organic carbon (DOC) in eutrophic water. Although ADOM is known to be readily transformed by microbes, the role of sunlight-induced photochemical process and the interactions between two processes on ADOM transformation remains unclear. In this study, three types of treatments for ADOM, including photochemical process under natural solar light (L treatment), microbial process (M treatment), and the simultaneous photochemical plus microbial process (L&M), were performed for 18 days. Our results showed that M treatment was more effective for the loss of DOC, chromophoric DOM (CDOM) at short wavelengths (a254 and a280), than L treatment, while L treatment was more effective for the transformation of a350 and the fluorescent components of the ubiquitous humic-like component and the tryptophan-like component. Comparison in the decay kinetics of DOC and CDOM in the three treatments showed that the simultaneous photochemical and biological processes exhibited an inhibitory effect on DOC decay rate but not the percentage of labile DOC fraction. Higher relative abundance of protein-like substances was found after L&M treatment, while the relative abundance of humic-like substance and aromaticity increased after M treatment, and the low molecular-weight compounds were produced after L treatment. Our results emphasized the importance of photochemistry in processing ADOM to mediate the chemodiversity in natural water.
Subject(s)
Dissolved Organic Matter , Sunlight , Water , Spectrometry, Fluorescence , Photochemical Processes , Humic Substances/analysisABSTRACT
Humic acid (HA) and phosphate interactions play a vital role in the biogeochemical cycle of carbon and nutrients and thus the trophic state of a lake. The adsorption behavior of HAs to sediments in the absence and presence of phosphate was investigated in this study. Three types of HAs were used, AHA from algae-dominated lake sediments, MHA from macrophyte-dominated lake sediments, and a reference HA (RHA) with terrestrial sources. The adsorption capacity of lake sediments was highest for AHA, which can be explained by that AHA contained more carboxyl-containing molecules, proteinaceous compounds and polysaccharides that were preferentially adsorbed by minerals. Phosphate showed a stronger inhibitory effect on MHA adsorption than on AHA adsorption, suggesting that AHA can more effectively replace phosphate adsorbed to sediments. Our findings show that the functional groups of organic compounds control not only their fractionation and burial but also their ability to replace phosphate in sediments. We propose a novel mechanism to explain the legacy effect of lake eutrophication. That is, as lakes shift from a macrophyte-dominated state to more eutrophic, algae-dominated state, increasing algae-derived organic compounds can promote the release of phosphate from sediments, forming a positive feedback loop that sustains internal phosphorus loading and hence lake eutrophication.
Subject(s)
Lakes , Water Pollutants, Chemical , Adsorption , China , Environmental Monitoring , Eutrophication , Geologic Sediments/chemistry , Humic Substances/analysis , Lakes/chemistry , Phosphates , Phosphorus/analysis , Water Pollutants, Chemical/analysisABSTRACT
The generation of organic matter (OM) occurs synchronously with phytoplankton growth. Characterization of the generated particulate and dissolved OM during algal blooms in eutrophic lakes is crucial for better understanding the carbon cycle but remains limited. We speculate that sediments play a critical role in the biogeochemical transformation of OM derived from algal blooms in shallow lakes. In this study, changes in OM quantity and quality and the concentrations of biogenic elements (nutrients and metals) during algal blooms, were studied in situ in a shallow eutrophic lake (Lake Chaohu, China). Two enclosure treatments in the presence and absence of sediments were compared, and the cause-effect relationships among sediment, nutrients, metals, phytoplankton, particulate OM (POM), and dissolved OM (DOM) were revealed by a partial least square-path model (PLS-PM). The results showed that the changes in nutrients and metals concentrations over time were consistent with that of chlorophyll a (Chl a), and at the end of the treatment, the concentrations of Chl a, nutrients, and metals in Treatment S (with sediments) were approximately 3-5 times of those in Treatment N (without sediments). The high concentration of Chl a in Treatment S resulted in a high quantity of POM, which showed low molecular weight, low humification, and was enriched in protein-like components (â¼ 70%). For DOM, the quantity increased after the decrease in POM, and DOM quality showed a significantly higher abundance of humic-like components and a higher molecular weight than POM did. The PLS-PM results showed that the significant positive effects of sediment on nutrients, metals, phytoplankton, POM, and DOM were 0.28, 0.37, 0.28, 0.25, and 0.25, respectively, suggesting that sediment had an important role in the biogeochemical cycles of these substances. The significant negative relationship between POM and DOM (-0.62) and the distinct difference in POM and DOM quality implied the efficient transformation of the freshly generated OM to those with a higher molecular weight, higher humification, and potentially refractory. Our results depicted the quick biogeochemical transformation of nutrients, metals, and the potential formation of refractory organic carbon in water column, as driven by the couple of the algae pump with the microbial carbon pump.
Subject(s)
Geologic Sediments , Lakes , Carbon , China , Chlorophyll A , Eutrophication , Lakes/chemistry , PhytoplanktonABSTRACT
Macrophyte- and algae-dominated lakes (zones) are the two typical states of shallow lakes, where the source and composition of organic matter are distinct. The burial of organic matter (OM) in the sediment supports the role of lakes as carbon sinks. However, organic matter in the sediments could be further processed, influencing the carbon cycle. The post-burial metabolism of the sedimentary OM relates closely to its composition. However, information on the differences in composition remains limited, especially the molecular composition of organic matter from sediments in the macrophyte-dominated and algae-dominated lakes. In this study, sediments were collected from the macrophyte-dominated and algae-dominated zones of Taihu Lake (East Taihu Lake and Meiliang Bay, respectively), and the active pool of sedimentary OM (water soluble organic matter, WSOM) was extracted and purified. The composition of the WSOM was characterized in detail via absorption spectroscopy, fluorescent spectroscopy, infrared spectroscopy, and Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR MS). The optical index of E2:E3 showed that the molecular size of WSOM in the macrophyte-dominated zone (M-WSOM) was slightly larger than that in the algae-dominated zone (A-WSOM). Consistently, the intensity-weighted molecular weights were identified as 388.9 and 379.9, respectively, via FT-ICR MS analysis. M-WSOM was more humified than A-WSOM, as evidenced by the SUVA254 and HIX values. The FT-ICR MS results showed that the relative abundance of the condensed aromatic substance and the aromatics were 6.3% (intensity-weighted) and 7.7% for M-WSOM and 1.1% and 4.4% for A-WSOM, respectively. The excitation-emission matrix fluorescence-parallel factor analysis (EEM-PARAFAC) suggested that the protein-like component was more in A-WSOM than that in M-WSOM, and the FT-ICR MS results showed that the intensity-weighted relative abundances of peptides were 35.6% and 15.6% for A-WSOM and M-WSOM, respectively. The FT-ICR MS results further showed that the heteroatom-containing molecules were abundant in the sedimentary WSOM, i.e., 82.9% and 91.7% for M-WSOM and A-WSOM, respectively. The nitrogen-containing molecules dominated, contributing to 53.5% and 78.5% of M-WSOM and A-WSOM, respectively. There were 30.4% and 41.4% phosphorus-containing molecules in M-WSOM and A-WSOM, respectively. The phosphorus-containing molecules in M-WSOM were mainly aliphatics and highly unsaturated structures with low oxygen, whereas those in A-WSOM were mainly peptides. This study elucidated the detailed molecular composition of WSOM in the macrophyte-dominated and algae-dominated zones of Taihu Lake, which aids understanding of the carbon, nitrogen, and phosphorus biogeochemical cycles in lakes.
Subject(s)
Geologic Sediments , Lakes , China , Environmental Monitoring/methods , Geologic Sediments/chemistry , Lakes/chemistry , Nitrogen/analysis , Phosphorus/analysis , Spectrum Analysis , Water/analysisABSTRACT
Human activities, such as land use change and eutrophication, threaten freshwater biodiversity and ecosystem function. In this study, we examined both the α- and ß-diversity of plankton communities, that is, bacteria/prokaryotic algae, eukaryotic algae, and zooplankton/metazoans, using both classical microscopy and high-throughput sequencing methods across 40 lakes of the Yangtze River Basin. The spatial variations in plankton communities were explained by environmental variables such as trophic status index (TSI) and environmental heterogeneity according to non-metric multidimensional scaling analyses, mantel tests, and structural equation model. Our results showed that the compositional dissimilarities of bacteria, cyanobacteria, eukaryotic algae, and metazoans all decreased with the increasing TSI values, and were significantly positively related to environmental dissimilarity. Both the species richness and compositional dissimilarity of zooplankton had positive effects on zooplankton/phytoplankton biomass ratio. Zooplankton diversity was not directly affected by TSI and environmental dissimilarity; however, it was indirectly affected by the biotic interactions with cyanobacteria or eukaryotic algae. In addition, there were significant positive relationships between bacteria/cyanobacteria and eukaryotic algae dissimilarities. Our results indicated that increased trophic status and decreased environmental dissimilarity as consequences of eutrophication may weaken the trophic cascading effects of planktonic food chain via reducing the top-down effects of zooplankton on phytoplankton.
Subject(s)
Cyanobacteria , Eutrophication , Plankton , Animals , Biomass , Ecosystem , Food Chain , Lakes , Phytoplankton , ZooplanktonABSTRACT
A large amount of intracellular dissolved organic matter (I-DOM) is released during the senescent phase of phytoplankton cultures. This research investigated the bio-incubation of I-DOM of cyanobacteria in Lake Taihu under various temperatures (20, 25, and 30â) and I-DOM initial concentrations (5, 10, and 20 mg·L-1) with the aid of ultraviolet-visible spectroscopy (UV-Vis) and three-dimensional fluorescence matrix-parallel factor (EEM-PARAFAC). I-DOM was effectively degraded during the incubation. After 14 days, the DOC removal ratio was 50% ~74%. A tryptophan-like component (C1), a ubiquitous humic-like component (C2), and two microbially-derived humic-like components (C3 and C4) contributed 80.0%, 16.0%, 3.7%, and 0.3% to the initial I-DOM, respectively. During the bio-degradation, these components are not only consumed but also produced. C1 decreased during the incubation, while C3 and C4 increased at the beginning of biodegradation and then decreased. The change trend of C2 was complicated, i.e., it decreased firstly and then increased, but decreased again after 7 days. The changes in the optical indices of Sr, E2:E3 and HIX revealed that the molecular weight of DOM increased, and the aromaticity was enhanced during degradation. The reaction temperature and the initial concentration of I-DOM did not change the trend of the PARAFAC components. The temperature of 25â was the most suitable for I-DOM bio-degradation. Additionally, the degradation of I-DOM was enhanced with the increase in the initial concentration of I-DOM. Combined with our study on the photodegradation of I-DOM, the possible fate of I-DOM in Lake Taihu was proposed. The tryptophan-like compound could be effectively degraded, while the humic-like components could not be degraded completely. These humic-like components would potentially settle through adsorption or coprecipitation with metal substances. These results are helpful to understand the fate of I-DOM released by a cyanobacteria bloom in Lake Taihu.
Subject(s)
Cyanobacteria , Dissolved Organic Matter , Lakes , Biodegradation, Environmental , Factor Analysis, Statistical , Humic Substances/analysis , Spectrometry, FluorescenceABSTRACT
Agricultural land use leads to significant changes in both the quality (e.g., sources and compositions) and quantity of dissolved organic matter (DOM) exported from terrestrial to aquatic ecosystems. However, the effect of agricultural activities often interacts with those of hydroclimatic drivers, making it difficult to delineate agriculture-induced changes and identify associated mechanisms. Using partial least square path modeling (PLS-PM), we examined the relative importance of agricultural land use, stream order, precipitation, and temperature in mediating allochthonous versus autochthonous sources and pathways that influenced stream DOM quality and quantity. We analyzed stream water DOM from 15 small streams draining watersheds across a gradient of agricultural land use in Southeast USA for about one year. For DOM quantity, agricultural land use increased the export of DOC and various DOM pools (terrestrial humic, microbial humic, and protein-like DOM) from land to streams, and for DOM quality, agricultural streams showed greater proportions of microbial humic compounds than forested streams. The PLS-PM model for DOM quantity accounted for 75.5% of total variance and identified that agricultural land use increased stream water DOM quantity primarily through increasing allochthonous inputs, which can be attributed to shallower flow paths in agricultural watersheds that enabled the export of organic materials from the upper, organic-rich soil horizon. PLS-PM models for DOM quality only explained ~13% of the total variance, highlighting the complex dynamics between environmental drivers and stream water DOM. Relative to commonly used multivariate statistic modeling (e.g., redundancy analysis (RDA)), PLS-PM models offer the advantages of identifying the primary pathway by which agricultural lands alter freshwater DOM and quantifying the relative importance of interactive effects of agriculture and hydroclimatic drivers. Therefore, structural equation modeling is a powerful tool that should be more widely adopted to distinguish among multiple drivers and mechanisms regulating freshwater biogeochemistry.
Subject(s)
Rivers , Soil , Agriculture , Ecosystem , ForestsABSTRACT
Human activities can alter dissolved organic matter (DOM) in lakes through both direct (i.e., exporting DOM of anthropogenic sources) and indirect effects (i.e., enhancing the autochthonous production of DOM via nutrient loading). Distinguishing between the direct and indirect effects is important to better understand human impacts on aquatic systems, but it remains highly challenging due to the interdependence of associated environmental variables. Here, we demonstrated that disentangling the direct and indirect effects can be achieved through combining large-scale environmental monitoring with the Partial Least Squares Path Modeling (PLS-PM). We presented DOM data from 61 lakes within the floodplain of the Yangtze River (Lakes-YR), China, a region that has been subjected to intense anthropogenic disturbances. We analyzed the amount and composition of DOM through dissolved organic carbon (DOC), chromophoric DOM (CDOM), and fluorescent DOM (FDOM). Four fluorescence components were identified, including one tyrosine-like component, one tryptophan-like component, and two humic-like components. Most of the lakes were dominated by freshly produced DOM with small molecular weights and low humification. Results from the PLS-PM models showed that the autochthonous production was more important than anthropogenic inputs in mediating DOC and CDOM. In contrast, FDOM parameters in lakes were more sensitive to the direct, anthropogenic sources, including treated domestic, industrial wastewater, and the effluents of aquaculture. These sources can be identified by elevated FDOM content per DOC (FDOM: DOC ratio) relative to autochthonous DOM, suggesting the potential of using FDOM as a tracer to identify and monitor the contribution of anthropogenic organic matter to inland waters.
ABSTRACT
Dissolved organic matter (DOM) plays important roles in the aquatic biogeochemical cycle and the global carbon cycle. However, it is highly spatially and temporally varied due to complex sources from the catchment (allochthonous) and from within the system (autochthonous). Satellite remote sensing provides the ability to monitor DOM and identify the spatio-temporal variations in lakes on a global or regional scale. In this study, field work was conducted in 55 lakes in August 2012 along the middle and lower reaches of the Yangtze River (MLR-YR), where most lakes were characterized by eutrophication due to intense human activities. The results showed that both colored DOM (CDOM) and total DOM differed significantly by and were linearly related to the human-induced trophic state index (TSI), with R2â¯=â¯0.41 and 0.61, respectively. Autochthonous substances by phytoplankton contributed to 38.5% of CDOM and 35.2% of DOM, and allochthonous terrestrial substance indexed by land cover change and aquaculture contributed to almost half, with 49.7% of CDOM and 49.8% of DOM. In total, human activities explained as much as 81.7% and 87.5% of the variations in CDOM and DOM, respectively. Finally, a flowchart for estimating DOM from satellite-derived TSI was proposed. This study has great significance for synchronously monitoring and managing aquatic environment quality in regional eutrophic lakes around the world.
Subject(s)
Lakes , Rivers , China , Environmental Monitoring , Eutrophication , Human Activities , Humans , PhytoplanktonABSTRACT
Hydroxyl radical (HOâ) in natural waters plays a critical role in contaminant transformation and ecosystem health. In this study, the photogeneration and steady-state concentration of HOâ in different aquatic environments (e.g., river and lake) along the middle-lower Yangtze region, China, were evaluated. The results showed that, compared to lake samples, the river waters were characterized by lower HOâ photoformation rate (RHOâ) (5.10-11.69 × 10-11 vs. 1.10-1.82 × 10-10 M s-1) and steady-state HOâ concentration ([HOâ]) (1.76-3.11 × 10-17 vs. 2.50-10.33 × 10-17 M). The contribution of nitrate and nitrite to the total RHOâ in river waters was generally higher than that in lake waters, and photolysis of nitrite exhibited contributions 1-2 times higher than those of nitrate (0-25% vs. 0-9%) irrespective of sample types. As a result, the photosensitization by chromophoric dissolved organic matter (CDOM) contributed more than 70% of the total RHOâ for all samples except for River Ganjiang. [HOâ] among all samples was positively correlated with dissolved organic carbon (DOC) concentration, and the DOC-normalized [HOâ] was further related to the physicochemical properties of CDOM samples (e.g., aromaticity, humification, and molecular weight). The humic-like aromatic substances with low molecular weight were the controlling factors influencing [HOâ] in the studied surface waters. The results contributed to a deeper understanding of behaviors and fate of aquatic DOMs in terms of HOâ formation and contaminant attenuation.
Subject(s)
Hydroxyl Radical , Rivers , China , Ecosystem , LakesABSTRACT
The rapid development and exploitation of the Yangtze River basin in order to ensure human food security and increase living space in recent decades has resulted in significant potential for degradation of water quality in the river and in hundreds of lakes. Understanding how lake environments have evolved to their present state under a variety of external influences is crucial for evaluating their current status and anticipating future scenarios of environmental changes. However, the lakes along the middle reaches of the Yangtze River (MRY) are as yet little studied. Here, we described the long-term anthropogenic environmental transformations of a small lake (Lake Taibai) in the MRY area, based on a detailed quantitative geochemical analysis of the aliphatic hydrocarbons, nutrients (N and P), biogenic silica (BSi), and major and trace elements present in a dated sediment core retrieved from the lake. Our data revealed that levels of short-chain n-alkanes, αß-hopanes and the trace elements arsenic (As) and cadmium (Cd) were all low for the entire record in sediments prior to ca. 1970, reflecting unpolluted natural state of the lake. Pronounced anthropogenic effects began to appear in sediments deposited in the subsequent years ca. 1970-1990, during which the levels of all these components were elevated, most likely driven by input of nitrogen (N) and phosphorus (P) containing chemical fertilizers, pesticides and diesel oil respectively. Since ca. 1990, changes of short-chain n-alkane levels in the sediment suggested the lake had undergone dramatic eutrophication in which existing anthropogenic stressors were exacerbated by technological advances that extended the use of chemical fertilizer into aquaculture. This pattern contrasted with an otherwise comparable lake in the lower Yangtze River basin, Lake Changdang, in which trace element and petroleum pollution were much more prominent due to dramatic urbanization and industrialization of the catchment.
Subject(s)
Environmental Monitoring , Eutrophication , Fertilizers/toxicity , Geologic Sediments/analysis , Lakes/chemistry , Water Quality/standards , Aquaculture , China , Environmental Monitoring/methods , Fertilizers/analysis , Humans , Hydrocarbons/analysis , Nitrogen/analysis , Phosphorus/analysis , Trace Elements/analysis , Urbanization , Water Pollutants, Chemical/analysisABSTRACT
Applications of aluminium (Al) salt or lanthanum (La) modified bentonite (LMB) have become popular methodologies for immobilizing phosphorus (P) in eutrophic lakes. The presence of humic substances, has been shown to inhibit this form of treatment due to the complexation with La/Al. However, the effects of other dissolved organic matter (DOM), especially that derived from phytoplankton (the dominant source in eutrophic lakes) are unknown. In this study, the interaction with La/Al of Suwannee River Standard Humic Acid Standard II (SRHA) and algae-derived DOM (ADOM) were investigated and compared. Differed to SRHA which was dominated by polyphenol-like component (76.8%, C1-SRHA), majority in ADOM were protein-like substance, including 41.9% tryptophan-like component (C2-ADOM) and 21.0% tyrosine-like component (C3-ADOM). Two reactions of complexation and coprecipitation were observed between SRHA/ADOM and La/Al. Complexation dominated at low metal inputs less than 10⯵M and coprecipitation was the main reaction at higher metal inputs. For ADOM, the tryptophan-like component (C2-ADOM) was the important component to react with metal. The reaction rate for C2-ADOM with La were about two-third of that for C1-SRHA, indicating that the influence of C2-ADOM was significant during the P immobilization by La/Al-based treatment in eutrophic lakes. The P removal data in the presence of ADOM confirmed the significant inhibition of ADOM. In addition, based on the composition of coprecipitates and relatively biodegradable character of tryptophan-like substances (C2-ADOM), the coprecipitation of ADOM was assumed to reduce the stability of precipitated P in eutrophic lakes. The release of P from the potential biodegradation of the coprecipitates and thus the possible decline of the performance of P immobilization by La/Al-based treatments is an important work in the future.
Subject(s)
Aluminum/chemistry , Bentonite/chemistry , Eutrophication/physiology , Lakes/chemistry , Lanthanum/chemistry , Phosphorus/chemistry , Rivers/chemistry , Geologic Sediments/chemistry , Humic Substances/analysis , Ions , Phytoplankton , Spectrometry, Fluorescence/methodsABSTRACT
During the past few decades, the Yangtze River basin has undergone massive anthropogenic change. In order to evaluate the impacts of human interventions on sediment n-alkanes of lakes across this region, the aliphatic hydrocarbon fractions of 19 surface sediment samples collected from lakes along the middle reaches of the Yangtze River (MYR) were analyzed using gas chromatography-mass spectrometry. The n-alkanes extracted from the sediments contained a homologous series from C15 to C34, with a notable predominance of odd carbon compounds except for sediments from the more intensively industrialized Lake Daye, in which > C21 n-alkanes showed no odd/even predominance, and carbon preference index (CPI) approached unity. Abundance values of middle-chain (C21, C23, and C25) and long-chain (C27, C29, C31, and C33) n-alkanes in Lake Daye were approximately 4 to 3 times greater than the average for other lakes, reaching 272.4 and 486.3 µg/g TOC, respectively, in the study. Short-chain n-alkanes (C15, C17, and C19) in the sediments varied in abundance from 10.0 to 76.2 µg/g TOC across the study and showed a moderate correlation with total phosphorus (TP) concentrations in the overlying water. The results indicated anthropogenic eutrophication enhanced the accumulation of short-chain n-alkanes in sediments because the primary producers in which they are synthesized are highly susceptible to nutrient forcing. Middle-chain n-alkane abundances were less affected by eutrophication and generally enriched in macrophyte lakes, while long-chain n-alkanes tend to be low in sediments from more eutrophic water. In the case of Lake Daye, direct discharges of petroleum products from heavy industry have introduced quantities of petroleum n-alkanes (> C21), far exceeding the amounts of biogenic input, and the sediment > C21 n-alkanes detected in this study showed typical characteristics of petroleum source. In other lakes, inputs of petroleum products from surface runoff of vehicle/traffic emissions associated with urbanization and economic growth contributed comparatively few n-alkanes to sediments, resulting in declines in CPI for > C21 n-alkanes, most obviously in Lakes Huanggai, Donghu, and Futou. Calculated CPI values suggest that a major proportion of the n-alkanes present in these lakes are derived from biogenic input. The results of this study provided evidences that n-alkane profiles of lake sediments respond sensitively to human-induced eutrophication and different sources of petroleum pollution.
Subject(s)
Alkanes/analysis , Environmental Monitoring , Water Pollutants, Chemical/analysis , Carbon/analysis , China , Eutrophication , Gas Chromatography-Mass Spectrometry , Geologic Sediments/chemistry , Humans , Hydrocarbons/analysis , Lakes/chemistry , Organic Chemicals/analysis , Petroleum/analysis , Phosphorus/analysis , Rivers/chemistryABSTRACT
Human land use has led to significant changes in the character of dissolved organic matter (DOM) in lotic ecosystems. These changes are expected to have important environmental and ecological consequences. However, high spatiotemporal variability has been reported in previous studies, and the underlying mechanisms remain inadequately understood. This study assessed variation in the properties of stream water DOM within watersheds across a gradient of agricultural land use with grazing pasture lands as the dominant agricultural type in the southeastern United States. We collected water samples under baseflow conditions five times over eight months from a regional group of first- to fourth-order streams. Samples were analyzed for dissolved organic carbon (DOC) concentration, DOM quality based on absorbance and fluorescence properties, as well as DOM biodegradability. We found that air temperature and antecedent hydrological conditions (indicated by antecedent precipitation index and stream water sodium concentrations) positively influenced stream water DOC concentration, DOM fluorescence index, and the proportion of soil-derived, microbial humic fluorescence. This observation suggests that elevated production and release of microbial DOM in soils facilitated by high temperature, in conjunction with strong soil-stream hydrological connectivity, were important drivers for changes in the concentration and composition of stream water DOM. By comparison, watersheds with a high percentage of agricultural land use showed higher DOC concentration, larger proportion of soil-derived, humic-like DOM compounds, and higher DOC biodegradability. These observations reflect preferential mobilization of humic DOM compounds from shallow organic matter-rich soils in agricultural watersheds, likely due to enhanced soil erosion, organic matter oxidation and relatively shallow soil-to-stream flow paths.